Canonical Allele Identifier: CA8980807
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs745973015

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371431G>A , CM000680.2:g.60371431G>A GRCh38
NC_000018.9:g.58038664G>A , CM000680.1:g.58038664G>A GRCh37
NC_000018.8:g.56189644G>A NCBI36
NG_016441.1:g.6338C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.919C>T MANE Select ENSP00000299766.3:p.Gln307Ter
ENST00000299766.4:c.919C>T ENSP00000299766.3:p.Gln307Ter
NM_005912.2:c.919C>T NP_005903.2:p.Gln307Ter
NM_005912.3:c.919C>T MANE Select NP_005903.2:p.Gln307Ter