HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21001962A= , CM000664.2:g.21001962A= | GRCh38 |
NC_000002.11:g.21224834A= , CM000664.1:g.21224834A= | GRCh37 |
NC_000002.10:g.21078339A= | NCBI36 |
NG_011793.1:g.47112T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.13460T= MANE Select | ENSP00000233242.1:p.Ile4487= | |
ENST00000616098.4:c.13458T= | ENSP00000477990.1:n.13458T= | |
NM_000384.2:c.13460T= | NP_000375.2:p.Ile4487= | |
XM_011532809.1:c.5870-2689T= | XP_011531111.1:n.5870-2689T= | |
NM_000384.3:c.13460T= MANE Select | NP_000375.3:p.Ile4487= |