Linked Data
ClinVar Variation Id:
1546458
ClinVar RCV Id:
RCV003232530
dbSNP Id:
rs1351246894
gnomAD v2:
5-176687033-C-T
gnomAD v3:
5-177260032-C-T
gnomAD v4:
5-177260032-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177260032C>T , CM000667.2:g.177260032C>T | GRCh38 |
| NC_000005.9:g.176687033C>T , CM000667.1:g.176687033C>T | GRCh37 |
| NC_000005.8:g.176619639C>T | NCBI36 |
| NG_009821.1:g.131954C>T , LRG_512:g.131954C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508896.7:c.4137C>T | ENSP00000423372.3:p.Ala1379= | |
| ENST00000347982.9:c.4137C>T | ENSP00000343209.5:p.Ala1379= | |
| ENST00000354179.9:c.4137C>T | ENSP00000346111.5:p.Ala1379= | |
| ENST00000685206.1:n.4593C>T | ||
| ENST00000686993.1:c.4137C>T | ENSP00000510020.1:p.Ala1379= | |
| ENST00000687453.1:c.4701C>T | ENSP00000508426.1:p.Ala1567= | |
| ENST00000688613.1:n.4407C>T | ||
| ENST00000689345.1:c.4137C>T | ENSP00000509711.1:p.Ala1379= | |
| ENST00000689549.1:n.5157C>T | ||
| ENST00000439151.7:c.5010C>T MANE Select | ENSP00000395929.2:p.Ala1670= | |
| ENST00000347982.8:c.4203C>T | ENSP00000343209.4:p.Ala1401= | |
| ENST00000354179.8:c.4203C>T | ENSP00000346111.4:p.Ala1401= | |
| ENST00000439151.6:c.5010C>T | ENSP00000395929.2:p.Ala1670= | |
| NM_022455.4:c.5010C>T , LRG_512t1:c.5010C>T | NP_071900.2:p.Ala1670= | |
| NM_172349.2:c.4203C>T | NP_758859.1:p.Ala1401= | |
| XM_005265959.1:c.5010C>T | XP_005266016.1:p.Ala1670= | |
| XM_005265960.1:c.4203C>T | XP_005266017.1:p.Ala1401= | |
| XM_005265961.1:c.4203C>T | XP_005266018.1:p.Ala1401= | |
| XM_005265962.3:c.504C>T | XP_005266019.1:p.Ala168= | |
| XM_011534610.1:c.5010C>T | XP_011532912.1:p.Ala1670= | |
| XM_011534611.1:c.5010C>T | XP_011532913.1:p.Ala1670= | |
| XM_011534612.1:c.4590C>T | XP_011532914.1:p.Ala1530= | |
| XM_011534613.1:c.3954C>T | XP_011532915.1:p.Ala1318= | |
| XM_011534614.1:c.5010C>T | XP_011532916.1:p.Ala1670= | |
| XM_011534617.1:c.744C>T | XP_011532919.1:p.Ala248= | |
| NM_001365684.1:c.4203C>T | NP_001352613.1:p.Ala1401= | |
| XM_024446150.1:c.5010C>T | XP_024301918.1:p.Ala1670= | |
| XM_024446151.1:c.5010C>T | XP_024301919.1:p.Ala1670= | |
| XM_024446152.1:c.5010C>T | XP_024301920.1:p.Ala1670= | |
| XM_024446153.1:c.5010C>T | XP_024301921.1:p.Ala1670= | |
| XM_024446154.1:c.4590C>T | XP_024301922.1:p.Ala1530= | |
| XM_024446155.1:c.4203C>T | XP_024301923.1:p.Ala1401= | |
| XM_024446156.1:c.4203C>T | XP_024301924.1:p.Ala1401= | |
| XM_024446158.1:c.4203C>T | XP_024301926.1:p.Ala1401= | |
| XM_024446159.1:c.3954C>T | XP_024301927.1:p.Ala1318= | |
| XM_024446160.1:c.5010C>T | XP_024301928.1:p.Ala1670= | |
| XM_024446162.1:c.744C>T | XP_024301930.1:p.Ala248= | |
| XM_024446163.1:c.504C>T | XP_024301931.1:p.Ala168= | |
| NM_022455.5:c.5010C>T MANE Select | NP_071900.2:p.Ala1670= | |
| NM_172349.3:c.4203C>T | NP_758859.1:p.Ala1401= |