Canonical Allele Identifier: CA2307359170
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371856C= , CM000680.2:g.60371856C= GRCh38
NC_000018.9:g.58039089C= , CM000680.1:g.58039089C= GRCh37
NC_000018.8:g.56190069C= NCBI36
NG_016441.1:g.5913G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.494G= MANE Select ENSP00000299766.3:p.Arg165=
ENST00000299766.4:c.494G= ENSP00000299766.3:p.Arg165=
NM_005912.2:c.494G= NP_005903.2:p.Arg165=
NM_005912.3:c.494G= MANE Select NP_005903.2:p.Arg165=