HGVS | Genome Assembly |
---|---|
NC_000001.11:g.201317647G= , CM000663.2:g.201317647G= | GRCh38 |
NC_000001.10:g.201286775G= , CM000663.1:g.201286775G= | GRCh37 |
NC_000001.9:g.199553398G= | NCBI36 |
NG_023337.1:g.39196G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367324.8:c.922G= MANE Select | ENSP00000356293.4:p.Ala308= | |
ENST00000263946.7:c.922G= | ENSP00000263946.3:p.Ala308= | |
ENST00000352845.3:c.922G= | ENSP00000295597.3:p.Ala308= | |
ENST00000367324.7:c.922G= | ENSP00000356293.3:p.Ala308= | |
ENST00000475988.1:n.264G= | ||
ENST00000622031.4:c.919G= | ENSP00000482213.1:p.Ala307= | |
NM_000299.3:c.922G= | NP_000290.2:p.Ala308= | |
NM_001005337.2:c.922G= | NP_001005337.1:p.Ala308= | |
NM_001005337.3:c.922G= MANE Select | NP_001005337.1:p.Ala308= | |
NM_000299.4:c.922G= | NP_000290.2:p.Ala308= |