Canonical Allele Identifier: CA8980873
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs370022771
ExAC: 18:58038934 G / A
gnomAD v2: 18-58038934-G-A
gnomAD v3: 18-60371701-G-A
gnomAD v4: 18-60371701-G-A
MyVariant Identifiers: chr18:g.58038934G>A (hg19) chr18:g.60371701G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371701G>A , CM000680.2:g.60371701G>A GRCh38
NC_000018.9:g.58038934G>A , CM000680.1:g.58038934G>A GRCh37
NC_000018.8:g.56189914G>A NCBI36
NG_016441.1:g.6068C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.649C>T MANE Select ENSP00000299766.3:p.Leu217=
ENST00000299766.4:c.649C>T ENSP00000299766.3:p.Leu217=
NM_005912.2:c.649C>T NP_005903.2:p.Leu217=
NM_005912.3:c.649C>T MANE Select NP_005903.2:p.Leu217=
Search 100 bp 5'
Search 100 bp 3'