Canonical Allele Identifier: CA402719025
Gene: MC4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371536G>C , CM000680.2:g.60371536G>C GRCh38
NC_000018.9:g.58038769G>C , CM000680.1:g.58038769G>C GRCh37
NC_000018.8:g.56189749G>C NCBI36
NG_016441.1:g.6233C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.814C>G MANE Select ENSP00000299766.3:p.Pro272Ala
ENST00000299766.4:c.814C>G ENSP00000299766.3:p.Pro272Ala
NM_005912.2:c.814C>G NP_005903.2:p.Pro272Ala
NM_005912.3:c.814C>G MANE Select NP_005903.2:p.Pro272Ala