HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6044253C= , CM000674.2:g.6044253C= | GRCh38 |
NC_000012.11:g.6153419C= , CM000674.1:g.6153419C= | GRCh37 |
NC_000012.10:g.6023680C= | NCBI36 |
NG_009072.1:g.85418G= | |
NG_009072.2:g.85418G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.2442+38G= MANE Select | ENSP00000261405.5:n.2442+38G= | |
ENST00000261405.9:c.2442+38G= | ENSP00000261405.5:n.2442+38G= | |
ENST00000538635.5:n.421-50319G= | ||
NM_000552.3:c.2442+38G= | NP_000543.2:n.2442+38G= | |
NM_000552.4:c.2442+38G= | NP_000543.2:n.2442+38G= | |
NM_000552.5:c.2442+38G= MANE Select | NP_000543.3:n.2442+38G= |