Linked Data
ClinVar Variation Id:
48649
ClinVar RCV Id:
RCV000041970
dbSNP Id:
rs397514686
PubMed:
PMID:23561803
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.2915243G>A , CM000669.2:g.2915243G>A | GRCh38 |
| NC_000007.13:g.2954877G>A , CM000669.1:g.2954877G>A | GRCh37 |
| NC_000007.12:g.2921403G>A | NCBI36 |
| NG_027759.1:g.133633C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698637.1:n.3943C>T | ||
| ENST00000698652.1:n.1789C>T | ||
| ENST00000396946.9:c.2833C>T MANE Select | ENSP00000380150.4:p.Gln945Ter | |
| ENST00000396946.8:c.2833C>T | ENSP00000380150.4:p.Gln945Ter | |
| NM_032415.5:c.2833C>T | NP_115791.3:p.Gln945Ter | |
| XM_011515585.1:c.2833C>T | XP_011513887.1:p.Gln945Ter | |
| XM_011515586.1:c.2833C>T | XP_011513888.1:p.Gln945Ter | |
| XM_011515587.1:c.2830C>T | XP_011513889.1:p.Gln944Ter | |
| NM_001324281.1:c.2833C>T | NP_001311210.1:p.Gln945Ter | |
| XM_011515586.2:c.2833C>T | XP_011513888.1:p.Gln945Ter | |
| XM_011515587.2:c.2830C>T | XP_011513889.1:p.Gln944Ter | |
| NM_001324281.2:c.2833C>T | NP_001311210.1:p.Gln945Ter | |
| NM_032415.6:c.2833C>T | NP_115791.3:p.Gln945Ter | |
| NM_001324281.3:c.2833C>T | NP_001311210.1:p.Gln945Ter | |
| NM_032415.7:c.2833C>T MANE Select | NP_115791.3:p.Gln945Ter |