HGVS | Genome Assembly |
---|---|
NC_000002.12:g.98608279C>T , CM000664.2:g.98608279C>T | GRCh38 |
NC_000002.11:g.99224742C>T , CM000664.1:g.99224742C>T | GRCh37 |
NC_000002.10:g.98591174C>T | NCBI36 |
NG_031918.1:g.5240G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000328709.8:c.99+28G>A MANE Select | ENSP00000330730.3:n.99+28G>A | |
ENST00000328709.7:c.99+28G>A | ENSP00000330730.3:n.99+28G>A | |
ENST00000409997.1:c.99+28G>A | ENSP00000386934.1:n.99+28G>A | |
ENST00000483527.5:n.229G>A | ||
NM_001008215.2:c.99+28G>A | NP_001008216.1:n.99+28G>A | |
NM_001008215.3:c.99+28G>A MANE Select | NP_001008216.1:n.99+28G>A |