Linked Data
dbSNP Id:
rs1668089929
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26135346C>A , CM000664.2:g.26135346C>A | GRCh38 |
| NC_000002.11:g.26358215C>A , CM000664.1:g.26358215C>A | GRCh37 |
| NC_000002.10:g.26211719C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264710.5:c.*325C>A MANE Select | ENSP00000264710.4:n.*325C>A | |
| ENST00000264710.4:c.*325C>A | ENSP00000264710.4:n.*325C>A | |
| ENST00000495146.5:n.1291C>A | ||
| NM_016131.4:c.*325C>A | NP_057215.3:n.*325C>A | |
| XM_024452565.1:c.*325C>A | XP_024308333.1:n.*325C>A | |
| NM_016131.5:c.*325C>A MANE Select | NP_057215.3:n.*325C>A |