Linked Data
ClinVar Variation Id:
156410
ClinVar RCV Id:
RCV000144528
dbSNP Id:
rs587782998
PubMed:
PMID:25439098
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114651T>A , CM000667.2:g.140114651T>A | GRCh38 |
| NC_000005.9:g.139494236T>A , CM000667.1:g.139494236T>A | GRCh37 |
| NC_000005.8:g.139474420T>A | NCBI36 |
| NG_041813.1:g.5529T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.470T>A MANE Select | ENSP00000332706.3:p.Met157Lys | |
| ENST00000651386.1:c.470T>A | ENSP00000499133.1:p.Met157Lys | |
| ENST00000331327.4:c.470T>A | ENSP00000332706.3:p.Met157Lys | |
| NM_005859.4:c.470T>A | NP_005850.1:p.Met157Lys | |
| NM_005859.5:c.470T>A MANE Select | NP_005850.1:p.Met157Lys |