Canonical Allele Identifier: CA504305557
Gene: MC4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.58039457C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60372224C>T , CM000680.2:g.60372224C>T GRCh38
NC_000018.9:g.58039457C>T , CM000680.1:g.58039457C>T GRCh37
NC_000018.8:g.56190437C>T NCBI36
NG_016441.1:g.5545G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.126G>A MANE Select ENSP00000299766.3:p.Glu42=
ENST00000299766.4:c.126G>A ENSP00000299766.3:p.Glu42=
NM_005912.2:c.126G>A NP_005903.2:p.Glu42=
NM_005912.3:c.126G>A MANE Select NP_005903.2:p.Glu42=
Search 100 bp 5'
Search 100 bp 3'