HGVS | Genome Assembly |
---|---|
NC_000016.10:g.172947A>T , CM000678.2:g.172947A>T | GRCh38 |
NC_000016.9:g.222946A>T , CM000678.1:g.222946A>T | GRCh37 |
NC_000016.8:g.162946A>T | NCBI36 |
NG_000006.1:g.33810A>T | |
NG_059186.1:g.1297A>T | |
NG_059271.1:g.5101A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.35A>T MANE Select | ENSP00000251595.6:p.Lys12Met | |
ENST00000251595.10:c.35A>T | ENSP00000251595.6:p.Lys12Met | |
ENST00000397806.1:c.-13A>T | ENSP00000380908.1:n.-13A>T | |
ENST00000482565.1:n.54A>T | ||
ENST00000484216.1:n.4A>T | ||
NM_000517.4:c.35A>T | NP_000508.1:p.Lys12Met | |
NM_000517.6:c.35A>T MANE Select | NP_000508.1:p.Lys12Met |