HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81705471C>G , CM000665.2:g.81705471C>G | GRCh38 |
NC_000003.11:g.81754622C>G , CM000665.1:g.81754622C>G | GRCh37 |
NC_000003.10:g.81837312C>G | NCBI36 |
NG_011810.1:g.61330G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.286G>C MANE Select | ENSP00000410833.2:p.Glu96Gln | |
ENST00000429644.6:c.286G>C | ENSP00000410833.2:p.Glu96Gln | |
ENST00000489715.1:c.163G>C | ENSP00000419638.1:p.Glu55Gln | |
NM_000158.3:c.286G>C | NP_000149.3:p.Glu96Gln | |
NM_000158.4:c.286G>C MANE Select | NP_000149.4:p.Glu96Gln |