Canonical Allele Identifier: CA301530008
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs940167950

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371433C>T , CM000680.2:g.60371433C>T GRCh38
NC_000018.9:g.58038666C>T , CM000680.1:g.58038666C>T GRCh37
NC_000018.8:g.56189646C>T NCBI36
NG_016441.1:g.6336G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.917G>A MANE Select ENSP00000299766.3:p.Ser306Asn
ENST00000299766.4:c.917G>A ENSP00000299766.3:p.Ser306Asn
NM_005912.2:c.917G>A NP_005903.2:p.Ser306Asn
NM_005912.3:c.917G>A MANE Select NP_005903.2:p.Ser306Asn