Canonical Allele Identifier: CA402718659
Gene: MC4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371364G>T , CM000680.2:g.60371364G>T GRCh38
NC_000018.9:g.58038597G>T , CM000680.1:g.58038597G>T GRCh37
NC_000018.8:g.56189577G>T NCBI36
NG_016441.1:g.6405C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.986C>A MANE Select ENSP00000299766.3:p.Ser329Tyr
ENST00000299766.4:c.986C>A ENSP00000299766.3:p.Ser329Tyr
NM_005912.2:c.986C>A NP_005903.2:p.Ser329Tyr
NM_005912.3:c.986C>A MANE Select NP_005903.2:p.Ser329Tyr