HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413955G= , CM000665.2:g.119413955G= | GRCh38 |
NC_000003.11:g.119132802G= , CM000665.1:g.119132802G= | GRCh37 |
NC_000003.10:g.120615492G= | NCBI36 |
NG_007665.2:g.124583G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2026G= MANE Select | ENSP00000264245.4:p.Ala676= | |
ENST00000264245.8:c.2026G= | ENSP00000264245.4:p.Ala676= | |
NM_020754.3:c.2026G= | NP_065805.2:p.Ala676= | |
XM_005247671.3:c.1933G= | XP_005247728.1:p.Ala645= | |
XM_006713714.2:c.1966G= | XP_006713777.1:p.Ala656= | |
XM_006713714.3:c.1966G= | XP_006713777.1:p.Ala656= | |
XM_017006955.1:c.1534G= | XP_016862444.1:p.Ala512= | |
NM_020754.4:c.2026G= MANE Select | NP_065805.2:p.Ala676= |