Canonical Allele Identifier: CA2307359050
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371624C= , CM000680.2:g.60371624C= GRCh38
NC_000018.9:g.58038857C= , CM000680.1:g.58038857C= GRCh37
NC_000018.8:g.56189837C= NCBI36
NG_016441.1:g.6145G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.726G= MANE Select ENSP00000299766.3:p.Lys242=
ENST00000299766.4:c.726G= ENSP00000299766.3:p.Lys242=
NM_005912.2:c.726G= NP_005903.2:p.Lys242=
NM_005912.3:c.726G= MANE Select NP_005903.2:p.Lys242=