HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40285416C>T , CM000681.2:g.40285416C>T | GRCh38 |
NC_000019.9:g.40791323C>T , CM000681.1:g.40791323C>T | GRCh37 |
NC_000019.8:g.45483163C>T | NCBI36 |
NG_012038.2:g.4943G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578123.5:c.-85+32G>A | ENSP00000462022.1:n.-85+32G>A | |
XM_011526620.1:c.-85+32G>A | XP_011524922.1:n.-85+32G>A |