HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119415186C>G , CM000665.2:g.119415186C>G | GRCh38 |
NC_000003.11:g.119134033C>G , CM000665.1:g.119134033C>G | GRCh37 |
NC_000003.10:g.120616723C>G | NCBI36 |
NG_007665.2:g.125814C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.3257C>G MANE Select | ENSP00000264245.4:p.Ala1086Gly | |
ENST00000264245.8:c.3257C>G | ENSP00000264245.4:p.Ala1086Gly | |
NM_020754.3:c.3257C>G | NP_065805.2:p.Ala1086Gly | |
XM_005247671.3:c.3164C>G | XP_005247728.1:p.Ala1055Gly | |
XM_006713714.2:c.3197C>G | XP_006713777.1:p.Ala1066Gly | |
XM_006713714.3:c.3197C>G | XP_006713777.1:p.Ala1066Gly | |
XM_017006955.1:c.2765C>G | XP_016862444.1:p.Ala922Gly | |
NM_020754.4:c.3257C>G MANE Select | NP_065805.2:p.Ala1086Gly |