HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7525054G= , CM000681.2:g.7525054G= | GRCh38 |
NC_000019.9:g.7589940G= , CM000681.1:g.7589940G= | GRCh37 |
NC_000019.8:g.7495940G= | NCBI36 |
NG_015806.1:g.7445G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.125G= MANE Select | ENSP00000264079.5:p.Arg42= | |
ENST00000264079.10:c.125G= | ENSP00000264079.5:p.Arg42= | |
ENST00000394321.9:n.205G= | ||
ENST00000596390.1:n.241G= | ||
ENST00000601003.1:c.125G= | ENSP00000469074.1:p.Arg42= | |
NM_020533.2:c.125G= | NP_065394.1:p.Arg42= | |
NM_020533.3:c.125G= MANE Select | NP_065394.1:p.Arg42= |