Canonical Allele Identifier: CA2307358923
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371372A= , CM000680.2:g.60371372A= GRCh38
NC_000018.9:g.58038605A= , CM000680.1:g.58038605A= GRCh37
NC_000018.8:g.56189585A= NCBI36
NG_016441.1:g.6397T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.978T= MANE Select ENSP00000299766.3:p.Cys326=
ENST00000299766.4:c.978T= ENSP00000299766.3:p.Cys326=
NM_005912.2:c.978T= NP_005903.2:p.Cys326=
NM_005912.3:c.978T= MANE Select NP_005903.2:p.Cys326=