Canonical Allele Identifier: CA2307358976
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371478A= , CM000680.2:g.60371478A= GRCh38
NC_000018.9:g.58038711A= , CM000680.1:g.58038711A= GRCh37
NC_000018.8:g.56189691A= NCBI36
NG_016441.1:g.6291T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.872T= MANE Select ENSP00000299766.3:p.Ile291=
ENST00000299766.4:c.872T= ENSP00000299766.3:p.Ile291=
NM_005912.2:c.872T= NP_005903.2:p.Ile291=
NM_005912.3:c.872T= MANE Select NP_005903.2:p.Ile291=