HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942207A= , CM000672.2:g.94942207A= | GRCh38 |
NC_000010.10:g.96701964A= , CM000672.1:g.96701964A= | GRCh37 |
NC_000010.9:g.96691954A= | NCBI36 |
NG_008385.1:g.8550A= | |
NG_008385.2:g.9050A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.347A= MANE Select | ENSP00000260682.6:p.Asn116= | |
ENST00000643112.1:c.347A= | ENSP00000496202.1:p.Asn116= | |
ENST00000645207.1:n.500A= | ||
ENST00000260682.6:c.347A= | ENSP00000260682.6:p.Asn116= | |
ENST00000461906.1:n.372A= | ||
ENST00000473496.1:n.118A= | ||
NM_000771.3:c.347A= | NP_000762.2:p.Asn116= | |
NM_000771.4:c.347A= MANE Select | NP_000762.2:p.Asn116= |