Linked Data
ClinVar Variation Id:
10240
ClinVar RCV Id:
RCV000010953
dbSNP Id:
rs137852431
PubMed:
PMID:8449505
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154947854C>T , CM000685.2:g.154947854C>T | GRCh38 |
| NC_000023.10:g.154176129C>T , CM000685.1:g.154176129C>T | GRCh37 |
| NC_000023.9:g.153829323C>T | NCBI36 |
| NG_011403.1:g.79870G>A | |
| NG_011403.2:g.79870G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1957G>A MANE Select | ENSP00000353393.4:p.Val653Met | |
| ENST00000647125.1:c.*1779+6038G>A | ENSP00000496062.1:n.*1779+6038G>A | |
| ENST00000360256.8:c.1957G>A | ENSP00000353393.4:p.Val653Met | |
| NM_000132.3:c.1957G>A | NP_000123.1:p.Val653Met | |
| XM_011531126.1:c.1852G>A | XP_011529428.1:p.Val618Met | |
| NM_000132.4:c.1957G>A MANE Select | NP_000123.1:p.Val653Met |