HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919646G>T , CM000679.2:g.74919646G>T | GRCh38 |
NC_000017.10:g.72915741G>T , CM000679.1:g.72915741G>T | GRCh37 |
NC_000017.9:g.70427336G>T | NCBI36 |
NG_007882.1:g.8611C>A | |
NG_033062.1:g.372G>T | |
NG_007882.2:g.8618C>A | |
NG_033062.2:g.372G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1190C>A MANE Select | ENSP00000480279.1:p.Ala397Asp | |
ENST00000579243.1:c.*789C>A | ENSP00000462568.1:n.*789C>A | |
ENST00000614341.4:c.1190C>A | ENSP00000480279.1:p.Ala397Asp | |
NM_001282489.2:c.881C>A | NP_001269418.1:p.Ala294Asp | |
NM_173477.4:c.1190C>A | NP_775748.2:p.Ala397Asp | |
XM_011524296.1:c.881C>A | XP_011522598.1:p.Ala294Asp | |
XM_011524296.2:c.881C>A | XP_011522598.1:p.Ala294Asp | |
NM_173477.5:c.1190C>A MANE Select | NP_775748.2:p.Ala397Asp | |
NM_001282489.3:c.881C>A | NP_001269418.1:p.Ala294Asp |