HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928031T>A , CM000663.2:g.149928031T>A | GRCh38 |
NC_000001.10:g.149899923T>A , CM000663.1:g.149899923T>A | GRCh37 |
NC_000001.9:g.148166547T>A | NCBI36 |
NG_032777.1:g.5222A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-272A>T | ENSP00000271628.8:n.-272A>T | |
NM_005850.4:c.-272A>T | NP_005841.1:n.-272A>T |