Canonical Allele Identifier: CA2307359069
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371658C= , CM000680.2:g.60371658C= GRCh38
NC_000018.9:g.58038891C= , CM000680.1:g.58038891C= GRCh37
NC_000018.8:g.56189871C= NCBI36
NG_016441.1:g.6111G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.692G= MANE Select ENSP00000299766.3:p.Gly231=
ENST00000299766.4:c.692G= ENSP00000299766.3:p.Gly231=
NM_005912.2:c.692G= NP_005903.2:p.Gly231=
NM_005912.3:c.692G= MANE Select NP_005903.2:p.Gly231=