Linked Data
ClinVar Variation Id:
310611
ClinVar RCV Id:
RCV000282243
RCV000337086
RCV000350122
RCV000394763
RCV000399710
RCV000605884
RCV001245594
RCV004544544
dbSNP Id:
rs776360559
ExAC:
12:88500653 C / T
gnomAD v2:
12-88500653-C-T
gnomAD v3:
12-88106876-C-T
gnomAD v4:
12-88106876-C-T
COSMIC:
COSM4575770
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.88106876C>T , CM000674.2:g.88106876C>T | GRCh38 |
| NC_000012.11:g.88500653C>T , CM000674.1:g.88500653C>T | GRCh37 |
| NC_000012.10:g.87024784C>T | NCBI36 |
| NG_008417.1:g.40341G>A | |
| NG_008417.2:g.40341G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309041.12:c.2616G>A | ENSP00000308021.8:p.Ser872= | |
| ENST00000552810.6:c.2616G>A MANE Select | ENSP00000448012.1:p.Ser872= | |
| ENST00000672414.2:c.*787G>A | ENSP00000500729.1:n.*787G>A | |
| ENST00000673058.2:c.2616G>A | ENSP00000500665.2:p.Ser872= | |
| ENST00000674971.1:c.2616G>A | ENSP00000502194.1:p.Ser872= | |
| ENST00000675230.1:c.2595G>A | ENSP00000502503.1:p.Ser865= | |
| ENST00000675408.1:c.2616G>A | ENSP00000502298.1:p.Ser872= | |
| ENST00000675476.1:c.3477G>A | ENSP00000502161.1:p.Ser1159= | |
| ENST00000675628.1:n.2843G>A | ||
| ENST00000675794.1:c.*787G>A | ENSP00000502841.1:n.*787G>A | |
| ENST00000675833.1:c.3384G>A | ENSP00000502559.1:p.Ser1128= | |
| ENST00000676074.1:c.2616G>A | ENSP00000502079.1:p.Ser872= | |
| ENST00000676363.1:n.4679G>A | ||
| ENST00000676448.1:c.*529G>A | ENSP00000501987.1:n.*529G>A | |
| ENST00000309041.11:c.2622G>A | ENSP00000308021.7:p.Ser874= | |
| ENST00000552810.5:c.2616G>A | ENSP00000448012.1:p.Ser872= | |
| ENST00000604024.5:c.1875G>A | ENSP00000473863.1:p.Ser625= | |
| NM_025114.3:c.2616G>A | NP_079390.3:p.Ser872= | |
| XM_011538756.1:c.3477G>A | XP_011537058.1:p.Ser1159= | |
| XM_011538757.1:c.3477G>A | XP_011537059.1:p.Ser1159= | |
| XM_011538758.1:c.3477G>A | XP_011537060.1:p.Ser1159= | |
| XM_011538759.1:c.3477G>A | XP_011537061.1:p.Ser1159= | |
| XM_011538760.1:c.3477G>A | XP_011537062.1:p.Ser1159= | |
| XM_011538761.1:c.3477G>A | XP_011537063.1:p.Ser1159= | |
| XM_011538762.1:c.2709G>A | XP_011537064.1:p.Ser903= | |
| XM_011538763.1:c.2616G>A | XP_011537065.1:p.Ser872= | |
| XM_011538764.1:c.3477G>A | XP_011537066.1:p.Ser1159= | |
| XM_011538765.1:c.3477G>A | XP_011537067.1:p.Ser1159= | |
| XM_011538766.1:c.1938G>A | XP_011537068.1:p.Ser646= | |
| XM_011538756.3:c.3477G>A | XP_011537058.1:p.Ser1159= | |
| XM_011538757.3:c.3477G>A | XP_011537059.1:p.Ser1159= | |
| XM_011538758.3:c.3477G>A | XP_011537060.1:p.Ser1159= | |
| XM_011538759.2:c.3477G>A | XP_011537061.1:p.Ser1159= | |
| XM_011538760.2:c.3477G>A | XP_011537062.1:p.Ser1159= | |
| XM_011538761.2:c.3477G>A | XP_011537063.1:p.Ser1159= | |
| XM_011538762.3:c.2709G>A | XP_011537064.1:p.Ser903= | |
| XM_011538763.3:c.2616G>A | XP_011537065.1:p.Ser872= | |
| XM_011538764.3:c.3477G>A | XP_011537066.1:p.Ser1159= | |
| XM_011538765.3:c.3477G>A | XP_011537067.1:p.Ser1159= | |
| XM_011538766.3:c.1938G>A | XP_011537068.1:p.Ser646= | |
| XM_017019980.2:c.3477G>A | XP_016875469.1:p.Ser1159= | |
| XM_017019981.2:c.3477G>A | XP_016875470.1:p.Ser1159= | |
| XM_017019982.1:c.3477G>A | XP_016875471.1:p.Ser1159= | |
| XM_017019983.2:c.2595G>A | XP_016875472.1:p.Ser865= | |
| XR_001748869.1:n.3821G>A | ||
| XR_001748870.2:n.3821G>A | ||
| NM_025114.4:c.2616G>A MANE Select | NP_079390.3:p.Ser872= |