HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270005C>G , CM000668.2:g.31270005C>G | GRCh38 |
NC_000006.11:g.31237782C>G , CM000668.1:g.31237782C>G | GRCh37 |
NC_000006.10:g.31345761C>G | NCBI36 |
NG_029422.2:g.7127G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.976G>C MANE Select | ENSP00000365402.5:p.Ala326Pro | |
ENST00000376228.9:c.976G>C | ENSP00000365402.5:p.Ala326Pro | |
ENST00000376237.8:c.*563G>C | ENSP00000365412.4:n.*563G>C | |
ENST00000383329.7:c.976G>C | ENSP00000372819.3:p.Ala326Pro | |
ENST00000470363.5:n.294G>C | ||
ENST00000487245.5:n.1335G>C | ||
NM_002117.5:c.976G>C | NP_002108.4:p.Ala326Pro | |
NM_002117.6:c.976G>C MANE Select | NP_002108.4:p.Ala326Pro |