HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40097474C>A , CM000663.2:g.40097474C>A | GRCh38 |
NC_000001.10:g.40563146C>A , CM000663.1:g.40563146C>A | GRCh37 |
NC_000001.9:g.40335733C>A | NCBI36 |
NG_009192.1:g.4997G>T , LRG_690:g.4997G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000433473.7:c.-236G>T | ENSP00000394863.3:n.-236G>T |