HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687328C>G , CM000671.2:g.136687328C>G | GRCh38 |
NC_000009.11:g.139581780C>G , CM000671.1:g.139581780C>G | GRCh37 |
NC_000009.10:g.138701601C>G | NCBI36 |
NG_008090.1:g.5132G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.30G>C MANE Select | ENSP00000360761.2:p.Ala10= | |
ENST00000371694.7:c.30G>C | ENSP00000360759.3:p.Ala10= | |
ENST00000371696.6:c.30G>C | ENSP00000360761.2:p.Ala10= | |
ENST00000470861.1:n.38G>C | ||
ENST00000538402.1:c.30G>C | ENSP00000438919.1:p.Ala10= | |
NM_001012727.1:c.30G>C | NP_001012745.1:p.Ala10= | |
NM_006412.3:c.30G>C | NP_006403.2:p.Ala10= | |
NM_006412.4:c.30G>C MANE Select | NP_006403.2:p.Ala10= | |
NM_001012727.2:c.30G>C | NP_001012745.1:p.Ala10= |