Canonical Allele Identifier: CA2307358935
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371392A= , CM000680.2:g.60371392A= GRCh38
NC_000018.9:g.58038625A= , CM000680.1:g.58038625A= GRCh37
NC_000018.8:g.56189605A= NCBI36
NG_016441.1:g.6377T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.958T= MANE Select ENSP00000299766.3:p.Tyr320=
ENST00000299766.4:c.958T= ENSP00000299766.3:p.Tyr320=
NM_005912.2:c.958T= NP_005903.2:p.Tyr320=
NM_005912.3:c.958T= MANE Select NP_005903.2:p.Tyr320=