Linked Data
ClinVar Variation Id:
386671
ClinVar RCV Id:
RCV000423115
RCV001112518
RCV001112517
RCV001112514
RCV001112515
RCV001112516
RCV001113853
RCV002393013
dbSNP Id:
rs750086412
ExAC:
12:110236533 G / A
gnomAD v2:
12-110236533-G-A
gnomAD v4:
12-109798728-G-A
COSMIC:
COSM4736748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109798728G>A , CM000674.2:g.109798728G>A | GRCh38 |
| NC_000012.11:g.110236533G>A , CM000674.1:g.110236533G>A | GRCh37 |
| NC_000012.10:g.108720916G>A | NCBI36 |
| NG_017090.1:g.39680C>T , LRG_372:g.39680C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261740.7:c.1038C>T MANE Select | ENSP00000261740.2:p.Tyr346= | |
| ENST00000418703.7:c.1038C>T | ENSP00000406191.2:p.Tyr346= | |
| ENST00000674908.1:c.*125C>T | ENSP00000502012.1:n.*125C>T | |
| ENST00000675533.1:n.1069C>T | ||
| ENST00000675670.1:c.1038C>T | ENSP00000502135.1:p.Tyr346= | |
| ENST00000676376.1:n.1069C>T | ||
| ENST00000261740.6:c.1038C>T | ENSP00000261740.2:p.Tyr346= | |
| ENST00000418703.6:c.1038C>T | ENSP00000406191.2:p.Tyr346= | |
| ENST00000536838.1:c.936C>T | ENSP00000444336.1:p.Tyr312= | |
| ENST00000537083.5:c.1038C>T | ENSP00000442738.1:p.Tyr346= | |
| ENST00000538125.5:c.1038C>T | ENSP00000437449.1:p.Tyr346= | |
| ENST00000541794.5:c.897C>T | ENSP00000442167.1:p.Tyr299= | |
| ENST00000544971.5:c.897C>T | ENSP00000443611.1:p.Tyr299= | |
| NM_001177428.1:c.897C>T | NP_001170899.1:p.Tyr299= | |
| NM_001177431.1:c.936C>T | NP_001170902.1:p.Tyr312= | |
| NM_001177433.1:c.897C>T | NP_001170904.1:p.Tyr299= | |
| NM_021625.4:c.1038C>T , LRG_372t1:c.1038C>T | NP_067638.3:p.Tyr346= | |
| NM_147204.2:c.1038C>T | NP_671737.1:p.Tyr346= | |
| XM_005253918.1:c.1038C>T | XP_005253975.1:p.Tyr346= | |
| XM_011538630.1:c.1038C>T | XP_011536932.1:p.Tyr346= | |
| XM_011538631.1:c.897C>T | XP_011536933.1:p.Tyr299= | |
| XM_011538632.1:c.1038C>T | XP_011536934.1:p.Tyr346= | |
| XM_011538633.1:c.897C>T | XP_011536935.1:p.Tyr299= | |
| XM_011538634.1:c.1038C>T | XP_011536936.1:p.Tyr346= | |
| XM_011538635.1:c.1191C>T | XP_011536937.1:p.Tyr397= | |
| XM_011538636.1:c.1191C>T | XP_011536938.1:p.Tyr397= | |
| XM_011538630.2:c.1191C>T | XP_011536932.2:p.Tyr397= | |
| XM_011538631.2:c.1050C>T | XP_011536933.2:p.Tyr350= | |
| XM_011538632.2:c.1191C>T | XP_011536934.2:p.Tyr397= | |
| XM_011538633.2:c.1050C>T | XP_011536935.2:p.Tyr350= | |
| XM_011538634.2:c.1191C>T | XP_011536936.2:p.Tyr397= | |
| XM_011538635.2:c.1191C>T | XP_011536937.1:p.Tyr397= | |
| XM_017019774.1:c.1038C>T | XP_016875263.1:p.Tyr346= | |
| NM_021625.5:c.1038C>T MANE Select | NP_067638.3:p.Tyr346= |