Canonical Allele Identifier: CA504305712
Gene: MC4R HGNC NCBI

Linked Data

gnomAD v4: 18-60372017-A-G
MyVariant Identifiers: chr18:g.58039250A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60372017A>G , CM000680.2:g.60372017A>G GRCh38
NC_000018.9:g.58039250A>G , CM000680.1:g.58039250A>G GRCh37
NC_000018.8:g.56190230A>G NCBI36
NG_016441.1:g.5752T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.333T>C MANE Select ENSP00000299766.3:p.Asp111=
ENST00000299766.4:c.333T>C ENSP00000299766.3:p.Asp111=
NM_005912.2:c.333T>C NP_005903.2:p.Asp111=
NM_005912.3:c.333T>C MANE Select NP_005903.2:p.Asp111=
Search 100 bp 5'
Search 100 bp 3'