Canonical Allele Identifier: CA2307359019
Gene: MC4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371567G= , CM000680.2:g.60371567G= GRCh38
NC_000018.9:g.58038800G= , CM000680.1:g.58038800G= GRCh37
NC_000018.8:g.56189780G= NCBI36
NG_016441.1:g.6202C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.783C= MANE Select ENSP00000299766.3:p.Phe261=
ENST00000299766.4:c.783C= ENSP00000299766.3:p.Phe261=
NM_005912.2:c.783C= NP_005903.2:p.Phe261=
NM_005912.3:c.783C= MANE Select NP_005903.2:p.Phe261=
Search 100 bp 5'
Search 100 bp 3'