HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269600T>G , CM000668.2:g.31269600T>G | GRCh38 |
NC_000006.11:g.31237377T>G , CM000668.1:g.31237377T>G | GRCh37 |
NC_000006.10:g.31345356T>G | NCBI36 |
NG_029422.2:g.7532A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1016-75A>C MANE Select | ENSP00000365402.5:n.1016-75A>C | |
ENST00000376228.9:c.1016-75A>C | ENSP00000365402.5:n.1016-75A>C | |
ENST00000376237.8:c.*603-75A>C | ENSP00000365412.4:n.*603-75A>C | |
ENST00000383329.7:c.1016-57A>C | ENSP00000372819.3:n.1016-57A>C | |
ENST00000466892.5:n.67A>C | ||
ENST00000470363.5:n.699A>C | ||
ENST00000487245.5:n.1375-75A>C | ||
NM_002117.5:c.1016-75A>C | NP_002108.4:n.1016-75A>C | |
NM_002117.6:c.1016-75A>C MANE Select | NP_002108.4:n.1016-75A>C |