Canonical Allele Identifier: CA402719029
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs121913562

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371538C>A , CM000680.2:g.60371538C>A GRCh38
NC_000018.9:g.58038771C>A , CM000680.1:g.58038771C>A GRCh37
NC_000018.8:g.56189751C>A NCBI36
NG_016441.1:g.6231G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.812G>T MANE Select ENSP00000299766.3:p.Cys271Phe
ENST00000299766.4:c.812G>T ENSP00000299766.3:p.Cys271Phe
NM_005912.2:c.812G>T NP_005903.2:p.Cys271Phe
NM_005912.3:c.812G>T MANE Select NP_005903.2:p.Cys271Phe