Canonical Allele Identifier: CA8980796
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs764575014

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371365A>G , CM000680.2:g.60371365A>G GRCh38
NC_000018.9:g.58038598A>G , CM000680.1:g.58038598A>G GRCh37
NC_000018.8:g.56189578A>G NCBI36
NG_016441.1:g.6404T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.985T>C MANE Select ENSP00000299766.3:p.Ser329Pro
ENST00000299766.4:c.985T>C ENSP00000299766.3:p.Ser329Pro
NM_005912.2:c.985T>C NP_005903.2:p.Ser329Pro
NM_005912.3:c.985T>C MANE Select NP_005903.2:p.Ser329Pro