HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928237C>A , CM000663.2:g.149928237C>A | GRCh38 |
NC_000001.10:g.149900129C>A , CM000663.1:g.149900129C>A | GRCh37 |
NC_000001.9:g.148166753C>A | NCBI36 |
NG_032777.1:g.5016G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-478G>T | ENSP00000271628.8:n.-478G>T | |
NM_005850.4:c.-478G>T | NP_005841.1:n.-478G>T |