HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40285474A>C , CM000681.2:g.40285474A>C | GRCh38 |
NC_000019.9:g.40791381A>C , CM000681.1:g.40791381A>C | GRCh37 |
NC_000019.8:g.45483221A>C | NCBI36 |
NG_012038.2:g.4885T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578123.5:c.-111T>G | ENSP00000462022.1:n.-111T>G | |
XM_011526620.1:c.-111T>G | XP_011524922.1:n.-111T>G |