HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787828T>A , CM000681.2:g.18787828T>A | GRCh38 |
NC_000019.9:g.18898637T>A , CM000681.1:g.18898637T>A | GRCh37 |
NC_000019.8:g.18759637T>A | NCBI36 |
NG_007070.1:g.8478A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.976-178A>T MANE Select | ENSP00000222271.2:n.976-178A>T | |
ENST00000222271.6:c.976-178A>T | ENSP00000222271.2:n.976-178A>T | |
ENST00000425807.1:c.817-178A>T | ENSP00000403792.1:n.817-178A>T | |
ENST00000542601.6:c.877-178A>T | ENSP00000439156.2:n.877-178A>T | |
NM_000095.2:c.976-178A>T | NP_000086.2:n.976-178A>T | |
NM_000095.3:c.976-178A>T MANE Select | NP_000086.2:n.976-178A>T |