Linked Data
ClinVar Variation Id:
433210
ClinVar RCV Id:
RCV000499280
dbSNP Id:
rs72653755
PubMed:
PMID:15894595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16208846C>T , CM000678.2:g.16208846C>T | GRCh38 |
| NC_000016.9:g.16302703C>T , CM000678.1:g.16302703C>T | GRCh37 |
| NC_000016.8:g.16210204C>T | NCBI36 |
| NG_007558.2:g.19626G>A | |
| NG_007558.3:g.19772G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000574094.6:c.676G>A | ENSP00000507301.1:p.Gly226Arg | |
| ENST00000622290.5:c.676G>A | ENSP00000483331.2:p.Gly226Arg | |
| ENST00000205557.12:c.676G>A MANE Select | ENSP00000205557.7:p.Gly226Arg | |
| ENST00000205557.11:c.676G>A | ENSP00000205557.7:p.Gly226Arg | |
| ENST00000456970.6:c.676G>A | ENSP00000405002.2:p.Gly226Arg | |
| ENST00000574094.5:n.772G>A | ||
| ENST00000577103.1:c.*543G>A | ENSP00000459243.1:n.*543G>A | |
| ENST00000622290.4:c.676G>A | ENSP00000483331.1:p.Gly226Arg | |
| NM_001171.5:c.676G>A | NP_001162.4:p.Gly226Arg | |
| XM_011522479.1:c.676G>A | XP_011520781.1:p.Gly226Arg | |
| XM_011522480.1:c.334G>A | XP_011520782.1:p.Gly112Arg | |
| XM_011522481.1:c.334G>A | XP_011520783.1:p.Gly112Arg | |
| XM_011522482.1:c.676G>A | XP_011520784.1:p.Gly226Arg | |
| XR_932836.1:n.911G>A | ||
| XR_932837.1:n.912G>A | ||
| XR_932838.1:n.912G>A | ||
| XR_933131.1:n.97-8C>T | ||
| XR_933132.1:n.97-8C>T | ||
| NM_001351800.1:c.334G>A | NP_001338729.1:p.Gly112Arg | |
| NR_147784.1:n.713G>A | ||
| XM_011522479.2:c.676G>A | XP_011520781.1:p.Gly226Arg | |
| XM_011522481.3:c.334G>A | XP_011520783.1:p.Gly112Arg | |
| XM_011522482.3:c.676G>A | XP_011520784.1:p.Gly226Arg | |
| XM_017023212.1:c.676G>A | XP_016878701.1:p.Gly226Arg | |
| XM_017023214.1:c.676G>A | XP_016878703.1:p.Gly226Arg | |
| XM_024450261.1:c.712G>A | XP_024306029.1:p.Gly238Arg | |
| XR_001752340.1:n.105-8C>T | ||
| XR_001752341.1:n.105-8C>T | ||
| XR_001752342.1:n.105-8C>T | ||
| XR_932836.2:n.857G>A | ||
| XR_932837.3:n.857G>A | ||
| XR_932838.3:n.857G>A | ||
| XR_933131.2:n.105-8C>T | ||
| XR_933132.2:n.105-8C>T | ||
| NM_001171.6:c.676G>A MANE Select | NP_001162.5:p.Gly226Arg |