HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136056748A= , CM000667.2:g.136056748A= | GRCh38 |
NC_000005.9:g.135392437A= , CM000667.1:g.135392437A= | GRCh37 |
NC_000005.8:g.135420336A= | NCBI36 |
NG_012646.1:g.32854A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000442011.7:c.1631A= MANE Select | ENSP00000416330.2:p.Asn544= | |
ENST00000442011.6:c.1631A= | ENSP00000416330.2:p.Asn544= | |
ENST00000506699.5:n.2148A= | ||
ENST00000507018.5:c.1609A= | ||
ENST00000509485.5:c.628A= | ||
ENST00000514242.5:n.402A= | ||
ENST00000514554.5:c.783A= | ||
NM_000358.2:c.1631A= | NP_000349.1:p.Asn544= | |
NM_000358.3:c.1631A= MANE Select | NP_000349.1:p.Asn544= |