Canonical Allele Identifier: CA301529995
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs1007984541
gnomAD v4: 18-60371289-A-T
MyVariant Identifiers: chr18:g.58038522A>T (hg19) chr18:g.60371289A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371289A>T , CM000680.2:g.60371289A>T GRCh38
NC_000018.9:g.58038522A>T , CM000680.1:g.58038522A>T GRCh37
NC_000018.8:g.56189502A>T NCBI36
NG_016441.1:g.6480T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.*62T>A MANE Select ENSP00000299766.3:n.*62T>A
ENST00000299766.4:c.*62T>A ENSP00000299766.3:n.*62T>A
NM_005912.3:c.*62T>A MANE Select NP_005903.2:n.*62T>A
Search 100 bp 5'
Search 100 bp 3'