HGVS | Genome Assembly |
---|---|
NC_000002.12:g.61378390T= , CM000664.2:g.61378390T= | GRCh38 |
NC_000002.11:g.61605525T= , CM000664.1:g.61605525T= | GRCh37 |
NC_000002.10:g.61459029T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398571.7:c.1049A= MANE Select | ENSP00000381577.2:p.Asn350= | |
ENST00000398571.6:c.1049A= | ENSP00000381577.2:p.Asn350= | |
ENST00000453133.1:c.575A= | ||
NM_014709.3:c.1049A= | NP_055524.3:p.Asn350= | |
NM_014709.4:c.1049A= MANE Select | NP_055524.3:p.Asn350= |