HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74920082C>A , CM000679.2:g.74920082C>A | GRCh38 |
NC_000017.10:g.72916177C>A , CM000679.1:g.72916177C>A | GRCh37 |
NC_000017.9:g.70427772C>A | NCBI36 |
NG_007882.1:g.8175G>T | |
NG_033062.1:g.808C>A | |
NG_007882.2:g.8182G>T | |
NG_033062.2:g.808C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.754G>T MANE Select | ENSP00000480279.1:p.Asp252Tyr | |
ENST00000579243.1:c.*353G>T | ENSP00000462568.1:n.*353G>T | |
ENST00000614341.4:c.754G>T | ENSP00000480279.1:p.Asp252Tyr | |
NM_001282489.2:c.445G>T | NP_001269418.1:p.Asp149Tyr | |
NM_173477.4:c.754G>T | NP_775748.2:p.Asp252Tyr | |
XM_011524296.1:c.445G>T | XP_011522598.1:p.Asp149Tyr | |
XM_011524296.2:c.445G>T | XP_011522598.1:p.Asp149Tyr | |
NM_173477.5:c.754G>T MANE Select | NP_775748.2:p.Asp252Tyr | |
NM_001282489.3:c.445G>T | NP_001269418.1:p.Asp149Tyr |