HGVS | Genome Assembly |
---|---|
NC_000005.10:g.78780500G>T , CM000667.2:g.78780500G>T | GRCh38 |
NC_000005.9:g.78076323G>T , CM000667.1:g.78076323G>T | GRCh37 |
NC_000005.8:g.78112079G>T | NCBI36 |
NG_007089.1:g.211035C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264914.10:c.1499C>A MANE Select | ENSP00000264914.4:p.Ser500Tyr | |
ENST00000264914.8:c.1499C>A | ENSP00000264914.4:p.Ser500Tyr | |
ENST00000521011.1:n.464C>A | ||
NM_000046.3:c.1499C>A | NP_000037.2:p.Ser500Tyr | |
XM_011543390.1:c.1499C>A | XP_011541692.1:p.Ser500Tyr | |
NM_000046.4:c.1499C>A | NP_000037.2:p.Ser500Tyr | |
NM_000046.5:c.1499C>A MANE Select | NP_000037.2:p.Ser500Tyr |