Canonical Allele Identifier: CA402720070
Gene: MC4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.58039262T>A (hg19) chr18:g.60372029T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60372029T>A , CM000680.2:g.60372029T>A GRCh38
NC_000018.9:g.58039262T>A , CM000680.1:g.58039262T>A GRCh37
NC_000018.8:g.56190242T>A NCBI36
NG_016441.1:g.5740A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.321A>T MANE Select ENSP00000299766.3:p.Leu107Phe
ENST00000299766.4:c.321A>T ENSP00000299766.3:p.Leu107Phe
NM_005912.2:c.321A>T NP_005903.2:p.Leu107Phe
NM_005912.3:c.321A>T MANE Select NP_005903.2:p.Leu107Phe
Search 100 bp 5'
Search 100 bp 3'