HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114716848A>T , CM000663.2:g.114716848A>T | GRCh38 |
NC_000001.10:g.115259469A>T , CM000663.1:g.115259469A>T | GRCh37 |
NC_000001.9:g.115060992A>T | NCBI36 |
NG_007572.1:g.5047T>A , LRG_92:g.5047T>A |
HGVS | Amino-acid Change |
---|---|
NM_002524.4:c.-208T>A | NP_002515.1:n.-208T>A |
ENST00000369535.4:c.-208T>A | ENSP00000358548.4:n.-208T>A |