Canonical Allele Identifier: CA8980818
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs754976323

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371468A>G , CM000680.2:g.60371468A>G GRCh38
NC_000018.9:g.58038701A>G , CM000680.1:g.58038701A>G GRCh37
NC_000018.8:g.56189681A>G NCBI36
NG_016441.1:g.6301T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.882T>C MANE Select ENSP00000299766.3:p.Asn294=
ENST00000299766.4:c.882T>C ENSP00000299766.3:p.Asn294=
NM_005912.2:c.882T>C NP_005903.2:p.Asn294=
NM_005912.3:c.882T>C MANE Select NP_005903.2:p.Asn294=