HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40285525C>A , CM000681.2:g.40285525C>A | GRCh38 |
NC_000019.9:g.40791432C>A , CM000681.1:g.40791432C>A | GRCh37 |
NC_000019.8:g.45483272C>A | NCBI36 |
NG_012038.2:g.4834G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578123.5:c.-162G>T | ENSP00000462022.1:n.-162G>T | |
XM_011526620.1:c.-162G>T | XP_011524922.1:n.-162G>T |