HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271261C>G , CM000668.2:g.31271261C>G | GRCh38 |
NC_000006.11:g.31239038C>G , CM000668.1:g.31239038C>G | GRCh37 |
NC_000006.10:g.31347017C>G | NCBI36 |
NG_029422.2:g.5871G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.431G>C MANE Select | ENSP00000365402.5:p.Gly144Ala | |
ENST00000376228.9:c.431G>C | ENSP00000365402.5:p.Gly144Ala | |
ENST00000376237.8:c.*18G>C | ENSP00000365412.4:n.*18G>C | |
ENST00000383329.7:c.431G>C | ENSP00000372819.3:p.Gly144Ala | |
ENST00000415537.1:c.429G>C | ||
ENST00000484378.1:n.700G>C | ||
ENST00000487245.5:n.790G>C | ||
ENST00000495835.1:n.620G>C | ||
NM_002117.5:c.431G>C | NP_002108.4:p.Gly144Ala | |
NM_002117.6:c.431G>C MANE Select | NP_002108.4:p.Gly144Ala |