HGVS | Genome Assembly |
---|---|
NC_000001.11:g.100539980G>A , CM000663.2:g.100539980G>A | GRCh38 |
NC_000001.10:g.101005536G>A , CM000663.1:g.101005536G>A | GRCh37 |
NC_000001.9:g.100778124G>A | NCBI36 |
NG_053134.1:g.6809G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000315033.5:c.1014G>A MANE Select | ENSP00000314223.4:p.Trp338Ter | |
ENST00000315033.4:c.1014G>A | ENSP00000314223.4:p.Trp338Ter | |
NM_022049.2:c.1014G>A | NP_071332.2:p.Trp338Ter | |
NM_022049.3:c.1014G>A MANE Select | NP_071332.2:p.Trp338Ter |