Canonical Allele Identifier: CA504305320
Gene: MC4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.58039349G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60372116G>T , CM000680.2:g.60372116G>T GRCh38
NC_000018.9:g.58039349G>T , CM000680.1:g.58039349G>T GRCh37
NC_000018.8:g.56190329G>T NCBI36
NG_016441.1:g.5653C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.234C>A MANE Select ENSP00000299766.3:p.Pro78=
ENST00000299766.4:c.234C>A ENSP00000299766.3:p.Pro78=
NM_005912.2:c.234C>A NP_005903.2:p.Pro78=
NM_005912.3:c.234C>A MANE Select NP_005903.2:p.Pro78=
Search 100 bp 5'
Search 100 bp 3'