Canonical Allele Identifier: CA402719175
Gene: MC4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371608T>G , CM000680.2:g.60371608T>G GRCh38
NC_000018.9:g.58038841T>G , CM000680.1:g.58038841T>G GRCh37
NC_000018.8:g.56189821T>G NCBI36
NG_016441.1:g.6161A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.742A>C MANE Select ENSP00000299766.3:p.Thr248Pro
ENST00000299766.4:c.742A>C ENSP00000299766.3:p.Thr248Pro
NM_005912.2:c.742A>C NP_005903.2:p.Thr248Pro
NM_005912.3:c.742A>C MANE Select NP_005903.2:p.Thr248Pro