HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928147C>T , CM000663.2:g.149928147C>T | GRCh38 |
NC_000001.10:g.149900039C>T , CM000663.1:g.149900039C>T | GRCh37 |
NC_000001.9:g.148166663C>T | NCBI36 |
NG_032777.1:g.5106G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-388G>A | ENSP00000271628.8:n.-388G>A | |
NM_005850.4:c.-388G>A | NP_005841.1:n.-388G>A |