Linked Data
ClinVar Variation Id:
313948
dbSNP Id:
rs116640707
ExAC:
14:73678523 C / T
gnomAD v2:
14-73678523-C-T
gnomAD v3:
14-73211815-C-T
gnomAD v4:
14-73211815-C-T
COSMIC:
COSM3690178
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.73211815C>T , CM000676.2:g.73211815C>T | GRCh38 |
| NC_000014.8:g.73678523C>T , CM000676.1:g.73678523C>T | GRCh37 |
| NC_000014.7:g.72748276C>T | NCBI36 |
| NG_007386.2:g.80345C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553599.6:c.990C>T | ENSP00000452477.2:p.Gly330= | |
| ENST00000554131.6:c.1002C>T | ENSP00000451915.2:p.Gly334= | |
| ENST00000554995.2:n.1752C>T | ||
| ENST00000555386.6:c.1082C>T | ENSP00000450845.1:p.Ala361Val | |
| ENST00000556066.2:n.1428C>T | ||
| ENST00000556951.6:c.990C>T | ENSP00000450551.2:p.Gly330= | |
| ENST00000557293.6:c.882C>T | ENSP00000451880.2:p.Gly294= | |
| ENST00000559361.6:c.*946C>T | ENSP00000454156.1:n.*946C>T | |
| ENST00000697912.1:c.990C>T | ENSP00000513477.1:p.Gly330= | |
| ENST00000697913.1:n.6552C>T | ||
| ENST00000700265.1:c.990C>T | ENSP00000514901.1:p.Gly330= | |
| ENST00000700266.1:c.*1214C>T | ENSP00000514902.1:n.*1214C>T | |
| ENST00000700267.1:c.1002C>T | ENSP00000514903.1:p.Gly334= | |
| ENST00000700268.1:c.1002C>T | ENSP00000514904.1:p.Gly334= | |
| ENST00000700269.1:c.1002C>T | ENSP00000514905.1:p.Gly334= | |
| ENST00000700271.1:c.944-5311C>T | ENSP00000514906.1:n.944-5311C>T | |
| ENST00000700272.1:c.*946C>T | ENSP00000514907.1:n.*946C>T | |
| ENST00000700273.1:c.990C>T | ENSP00000514908.1:p.Gly330= | |
| ENST00000700302.1:c.1002C>T | ENSP00000514929.1:p.Gly334= | |
| ENST00000700303.1:c.*664C>T | ENSP00000514930.1:n.*664C>T | |
| ENST00000700304.1:c.*946C>T | ENSP00000514931.1:n.*946C>T | |
| ENST00000700305.1:c.*560C>T | ENSP00000514932.1:n.*560C>T | |
| ENST00000700306.1:c.1002C>T | ENSP00000514933.1:p.Gly334= | |
| ENST00000700307.1:c.903C>T | ENSP00000514934.1:p.Gly301= | |
| ENST00000700308.1:c.*946C>T | ENSP00000514935.1:n.*946C>T | |
| ENST00000700309.1:c.*1091C>T | ENSP00000514936.1:n.*1091C>T | |
| ENST00000700310.1:c.983C>T | ENSP00000514937.1:p.Ala328Val | |
| ENST00000700311.1:c.1002C>T | ENSP00000514938.1:p.Gly334= | |
| ENST00000700312.1:c.753C>T | ENSP00000514939.1:p.Gly251= | |
| ENST00000700313.1:c.990C>T | ENSP00000514940.1:p.Gly330= | |
| ENST00000700314.1:c.*941C>T | ENSP00000514941.1:n.*941C>T | |
| ENST00000700315.1:c.*560C>T | ENSP00000514942.1:n.*560C>T | |
| ENST00000700316.1:c.*782C>T | ENSP00000514943.1:n.*782C>T | |
| ENST00000700317.1:c.1002C>T | ENSP00000514944.1:p.Gly334= | |
| ENST00000700318.1:c.*664C>T | ENSP00000514945.1:n.*664C>T | |
| ENST00000700319.1:c.*442C>T | ENSP00000514946.1:n.*442C>T | |
| ENST00000700320.1:c.1029C>T | ENSP00000514947.1:p.Gly343= | |
| ENST00000700321.1:c.1002C>T | ENSP00000514948.1:p.Gly334= | |
| ENST00000700322.1:c.990C>T | ENSP00000514949.1:p.Gly330= | |
| ENST00000700323.1:c.1002C>T | ENSP00000514950.1:p.Gly334= | |
| ENST00000700324.1:c.990C>T | ENSP00000514951.1:p.Gly330= | |
| ENST00000700375.1:c.1002C>T | ENSP00000514966.1:p.Gly334= | |
| ENST00000700377.1:c.*470C>T | ENSP00000514967.1:n.*470C>T | |
| ENST00000700378.1:c.1002C>T | ENSP00000514968.1:p.Gly334= | |
| ENST00000700379.1:n.1400C>T | ||
| ENST00000700389.1:c.990C>T | ENSP00000514970.1:p.Gly330= | |
| ENST00000700390.1:n.2713C>T | ||
| ENST00000700391.1:n.213C>T | ||
| ENST00000700404.1:n.2001C>T | ||
| ENST00000700435.1:n.1137C>T | ||
| ENST00000700436.1:c.1094C>T | ENSP00000514987.1:p.Ala365Val | |
| ENST00000700437.1:c.753C>T | ENSP00000514988.1:p.Gly251= | |
| ENST00000700468.1:c.891C>T | ENSP00000515001.1:p.Gly297= | |
| ENST00000700469.1:c.990C>T | ENSP00000515002.1:p.Gly330= | |
| ENST00000324501.10:c.1002C>T MANE Select | ENSP00000326366.5:p.Gly334= | |
| ENST00000324501.9:c.1002C>T | ENSP00000326366.5:p.Gly334= | |
| ENST00000357710.8:c.990C>T | ENSP00000350342.4:p.Gly330= | |
| ENST00000394164.5:c.990C>T | ENSP00000377719.1:p.Gly330= | |
| ENST00000406768.1:c.726C>T | ENSP00000385948.1:p.Gly242= | |
| ENST00000553855.5:c.1094C>T | ENSP00000452242.1:p.Ala365Val | |
| ENST00000554995.1:n.554C>T | ||
| ENST00000555386.5:c.1082C>T | ENSP00000450845.1:p.Ala361Val | |
| ENST00000555867.1:n.367C>T | ||
| ENST00000557511.5:c.956-5311C>T | ENSP00000451429.1:n.956-5311C>T | |
| NM_000021.3:c.1002C>T | NP_000012.1:p.Gly334= | |
| NM_007318.2:c.990C>T | NP_015557.2:p.Gly330= | |
| XM_005267864.1:c.1002C>T | XP_005267921.1:p.Gly334= | |
| XM_005267866.1:c.990C>T | XP_005267923.1:p.Gly330= | |
| XM_011536971.1:c.1002C>T | XP_011535273.1:p.Gly334= | |
| XM_011536972.1:c.1002C>T | XP_011535274.1:p.Gly334= | |
| XM_011536973.1:c.990C>T | XP_011535275.1:p.Gly330= | |
| XM_011536974.1:c.990C>T | XP_011535276.1:p.Gly330= | |
| XM_005267864.3:c.1002C>T | XP_005267921.1:p.Gly334= | |
| XM_005267866.2:c.990C>T | XP_005267923.1:p.Gly330= | |
| XM_011536972.2:c.1002C>T | XP_011535274.1:p.Gly334= | |
| XM_011536973.2:c.990C>T | XP_011535275.1:p.Gly330= | |
| XM_011536974.2:c.990C>T | XP_011535276.1:p.Gly330= | |
| NM_000021.4:c.1002C>T MANE Select | NP_000012.1:p.Gly334= | |
| NM_007318.3:c.990C>T | NP_015557.2:p.Gly330= |