Canonical Allele Identifier: CA301529996
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs189802778
gnomAD v2: 18-58038524-G-A
gnomAD v3: 18-60371291-G-A
gnomAD v4: 18-60371291-G-A
MyVariant Identifiers: chr18:g.58038524G>A (hg19) chr18:g.60371291G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371291G>A , CM000680.2:g.60371291G>A GRCh38
NC_000018.9:g.58038524G>A , CM000680.1:g.58038524G>A GRCh37
NC_000018.8:g.56189504G>A NCBI36
NG_016441.1:g.6478C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.*60C>T MANE Select ENSP00000299766.3:n.*60C>T
ENST00000299766.4:c.*60C>T ENSP00000299766.3:n.*60C>T
NM_005912.3:c.*60C>T MANE Select NP_005903.2:n.*60C>T
Search 100 bp 5'
Search 100 bp 3'