Linked Data
ClinVar Variation Id:
177692
dbSNP Id:
rs727504283
COSMIC:
COSM6007968
PubMed:
PMID:23074333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23431804G>A , CM000676.2:g.23431804G>A | GRCh38 |
| NC_000014.8:g.23901013G>A , CM000676.1:g.23901013G>A | GRCh37 |
| NC_000014.7:g.22970853G>A | NCBI36 |
| NG_007884.1:g.8858C>T , LRG_384:g.8858C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.596C>T MANE Select | ENSP00000347507.3:p.Ala199Val | |
| ENST00000355349.3:c.596C>T | ENSP00000347507.3:p.Ala199Val | |
| NM_000257.3:c.596C>T | NP_000248.2:p.Ala199Val | |
| XR_245686.3:n.702C>T | ||
| XM_017021340.1:c.596C>T | XP_016876829.1:p.Ala199Val | |
| NM_000257.4:c.596C>T MANE Select | NP_000248.2:p.Ala199Val |