Linked Data
ClinVar Variation Id:
536854
ClinVar RCV Id:
RCV000645535
RCV000856929
RCV001113399
RCV001113400
RCV001114786
RCV001114787
RCV001113398
RCV002458090
dbSNP Id:
rs145102919
ExAC:
12:110224531 G / A
gnomAD v2:
12-110224531-G-A
gnomAD v3:
12-109786726-G-A
gnomAD v4:
12-109786726-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109786726G>A , CM000674.2:g.109786726G>A | GRCh38 |
| NC_000012.11:g.110224531G>A , CM000674.1:g.110224531G>A | GRCh37 |
| NC_000012.10:g.108708914G>A | NCBI36 |
| NG_017090.1:g.51682C>T , LRG_372:g.51682C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261740.7:c.2320C>T MANE Select | ENSP00000261740.2:p.Arg774Cys | |
| ENST00000418703.7:c.2320C>T | ENSP00000406191.2:p.Arg774Cys | |
| ENST00000674908.1:c.*1407C>T | ENSP00000502012.1:n.*1407C>T | |
| ENST00000675670.1:c.2320C>T | ENSP00000502135.1:p.Arg774Cys | |
| ENST00000261740.6:c.2320C>T | ENSP00000261740.2:p.Arg774Cys | |
| ENST00000418703.6:c.2320C>T | ENSP00000406191.2:p.Arg774Cys | |
| ENST00000536838.1:c.2218C>T | ENSP00000444336.1:p.Arg740Cys | |
| ENST00000537083.5:c.2140C>T | ENSP00000442738.1:p.Arg714Cys | |
| ENST00000538125.5:c.*703C>T | ENSP00000437449.1:n.*703C>T | |
| ENST00000541794.5:c.2179C>T | ENSP00000442167.1:p.Arg727Cys | |
| ENST00000544971.5:c.1999C>T | ENSP00000443611.1:p.Arg667Cys | |
| NM_001177428.1:c.2179C>T | NP_001170899.1:p.Arg727Cys | |
| NM_001177431.1:c.2218C>T | NP_001170902.1:p.Arg740Cys | |
| NM_001177433.1:c.1999C>T | NP_001170904.1:p.Arg667Cys | |
| NM_021625.4:c.2320C>T , LRG_372t1:c.2320C>T | NP_067638.3:p.Arg774Cys | |
| NM_147204.2:c.2140C>T | NP_671737.1:p.Arg714Cys | |
| XM_005253918.1:c.2320C>T | XP_005253975.1:p.Arg774Cys | |
| XM_011538630.1:c.2320C>T | XP_011536932.1:p.Arg774Cys | |
| XM_011538631.1:c.2179C>T | XP_011536933.1:p.Arg727Cys | |
| XM_011538632.1:c.2140C>T | XP_011536934.1:p.Arg714Cys | |
| XM_011538633.1:c.1999C>T | XP_011536935.1:p.Arg667Cys | |
| XM_011538630.2:c.2473C>T | XP_011536932.2:p.Arg825Cys | |
| XM_011538631.2:c.2332C>T | XP_011536933.2:p.Arg778Cys | |
| XM_011538632.2:c.2293C>T | XP_011536934.2:p.Arg765Cys | |
| XM_011538633.2:c.2152C>T | XP_011536935.2:p.Arg718Cys | |
| XM_017019774.1:c.2320C>T | XP_016875263.1:p.Arg774Cys | |
| NM_021625.5:c.2320C>T MANE Select | NP_067638.3:p.Arg774Cys |