Canonical Allele Identifier: CA504305074
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs769947520

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371435C>G , CM000680.2:g.60371435C>G GRCh38
NC_000018.9:g.58038668C>G , CM000680.1:g.58038668C>G GRCh37
NC_000018.8:g.56189648C>G NCBI36
NG_016441.1:g.6334G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.915G>C MANE Select ENSP00000299766.3:p.Arg305=
ENST00000299766.4:c.915G>C ENSP00000299766.3:p.Arg305=
NM_005912.2:c.915G>C NP_005903.2:p.Arg305=
NM_005912.3:c.915G>C MANE Select NP_005903.2:p.Arg305=