HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6718276T>G , CM000681.2:g.6718276T>G | GRCh38 |
NC_000019.9:g.6718287T>G , CM000681.1:g.6718287T>G | GRCh37 |
NC_000019.8:g.6669287T>G | NCBI36 |
NG_009557.1:g.7376A>C , LRG_27:g.7376A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000594936.2:n.465A>C | ||
ENST00000695652.1:c.281A>C | ENSP00000512083.1:p.Asp94Ala | |
ENST00000695693.1:c.404A>C | ENSP00000512104.1:p.Asp135Ala | |
ENST00000245907.11:c.404A>C MANE Select | ENSP00000245907.4:p.Asp135Ala | |
ENST00000245907.10:c.404A>C | ENSP00000245907.4:p.Asp135Ala | |
ENST00000594936.1:n.465A>C | ||
ENST00000600744.1:c.281A>C | ENSP00000472044.1:p.Asp94Ala | |
NM_000064.3:c.404A>C | NP_000055.2:p.Asp135Ala | |
NM_000064.4:c.404A>C MANE Select | NP_000055.2:p.Asp135Ala |