Linked Data
ClinVar Variation Id:
360809
dbSNP Id:
rs4727267
gnomAD v2:
7-91570290-G-C
gnomAD v3:
7-91940976-G-C
gnomAD v4:
7-91940976-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.91940976G>C , CM000669.2:g.91940976G>C | GRCh38 |
| NC_000007.13:g.91570290G>C , CM000669.1:g.91570290G>C | GRCh37 |
| NC_000007.12:g.91408226G>C | NCBI36 |
| NG_011623.1:g.5102G>C , LRG_331:g.5102G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356239.8:c.-124G>C MANE Select | ENSP00000348573.3:n.-124G>C | |
| ENST00000679448.1:c.-124G>C | ENSP00000505889.1:n.-124G>C | |
| ENST00000679457.1:c.-124G>C | ENSP00000505450.1:n.-124G>C | |
| ENST00000679474.1:n.99G>C | ||
| ENST00000679521.1:c.-124G>C | ENSP00000505456.1:n.-124G>C | |
| ENST00000679554.1:c.-124G>C | ENSP00000506415.1:n.-124G>C | |
| ENST00000679722.1:n.99G>C | ||
| ENST00000679821.1:c.-124G>C | ENSP00000506040.1:n.-124G>C | |
| ENST00000680047.1:n.99G>C | ||
| ENST00000680072.1:c.-124G>C | ENSP00000506581.1:n.-124G>C | |
| ENST00000680074.1:n.99G>C | ||
| ENST00000680181.1:c.-124G>C | ENSP00000505548.1:n.-124G>C | |
| ENST00000680513.1:c.-124G>C | ENSP00000505284.1:n.-124G>C | |
| ENST00000680534.1:c.-124G>C | ENSP00000506674.1:n.-124G>C | |
| ENST00000680766.1:c.-124G>C | ENSP00000505204.1:n.-124G>C | |
| ENST00000680952.1:c.-124G>C | ENSP00000506407.1:n.-124G>C | |
| ENST00000681412.1:c.-124G>C | ENSP00000506486.1:n.-124G>C | |
| ENST00000681722.1:c.-124G>C | ENSP00000506566.1:n.-124G>C | |
| ENST00000356239.7:c.-124G>C | ENSP00000348573.3:n.-124G>C | |
| ENST00000394564.5:c.-124G>C | ENSP00000378065.1:n.-124G>C | |
| ENST00000493453.1:n.61G>C | ||
| ENST00000619023.4:c.-124G>C | ENSP00000480807.1:n.-124G>C | |
| NM_005751.4:c.-124G>C , LRG_331t1:c.-124G>C | NP_005742.4:n.-124G>C | |
| NM_147185.2:c.-124G>C | NP_671714.1:n.-124G>C | |
| XM_006715827.1:c.-124G>C | XP_006715890.1:n.-124G>C | |
| XM_011515709.1:c.-124G>C | XP_011514011.1:n.-124G>C | |
| XM_011515710.1:c.-124G>C | XP_011514012.1:n.-124G>C | |
| XM_011515711.1:c.-124G>C | XP_011514013.1:n.-124G>C | |
| XM_011515712.1:c.-124G>C | XP_011514014.1:n.-124G>C | |
| XM_011515713.1:c.-124G>C | XP_011514015.1:n.-124G>C | |
| XM_011515714.1:c.-124G>C | XP_011514016.1:n.-124G>C | |
| XM_011515716.1:c.-124G>C | XP_011514018.1:n.-124G>C | |
| XM_011515717.1:c.-124G>C | XP_011514019.1:n.-124G>C | |
| XM_011515718.1:c.-124G>C | XP_011514020.1:n.-124G>C | |
| XM_011515719.1:c.-124G>C | XP_011514021.1:n.-124G>C | |
| XM_011515720.1:c.-124G>C | XP_011514022.1:n.-124G>C | |
| XM_017011642.2:c.-124G>C | XP_016867131.1:n.-124G>C | |
| XM_017011643.2:c.-124G>C | XP_016867132.1:n.-124G>C | |
| XM_017011644.2:c.-124G>C | XP_016867133.1:n.-124G>C | |
| XM_017011645.2:c.-124G>C | XP_016867134.1:n.-124G>C | |
| XM_017011646.2:c.-124G>C | XP_016867135.1:n.-124G>C | |
| XM_017011647.2:c.-124G>C | XP_016867136.1:n.-124G>C | |
| XM_017011648.2:c.-124G>C | XP_016867137.1:n.-124G>C | |
| XM_017011649.2:c.-124G>C | XP_016867138.1:n.-124G>C | |
| XM_017011650.2:c.-124G>C | XP_016867139.1:n.-124G>C | |
| XM_017011651.2:c.-124G>C | XP_016867140.1:n.-124G>C | |
| XM_017011652.2:c.-124G>C | XP_016867141.1:n.-124G>C | |
| XM_017011653.2:c.-124G>C | XP_016867142.1:n.-124G>C | |
| XM_017011654.2:c.-124G>C | XP_016867143.1:n.-124G>C | |
| XM_024446631.1:c.-124G>C | XP_024302399.1:n.-124G>C | |
| NM_147185.3:c.-124G>C | NP_671714.1:n.-124G>C | |
| NM_005751.5:c.-124G>C MANE Select | NP_005742.4:n.-124G>C |