HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014138C>G , CM000663.2:g.1014138C>G | GRCh38 |
NC_000001.10:g.949518C>G , CM000663.1:g.949518C>G | GRCh37 |
NC_000001.9:g.939381C>G | NCBI36 |
NG_033033.1:g.5672C>G | |
NG_033033.2:g.18001C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000624697.4:c.134C>G | ENSP00000485643.1:p.Ala45Gly | |
ENST00000649529.1:c.158C>G MANE Select | ENSP00000496832.1:p.Ala53Gly | |
ENST00000379389.4:c.158C>G | ENSP00000368699.4:p.Ala53Gly | |
ENST00000624652.1:c.134C>G | ENSP00000485313.1:p.Ala45Gly | |
ENST00000624697.3:c.134C>G | ENSP00000485643.1:p.Ala45Gly | |
NM_005101.3:c.158C>G | NP_005092.1:p.Ala53Gly | |
NM_005101.4:c.158C>G MANE Select | NP_005092.1:p.Ala53Gly |