Canonical Allele Identifier: CA504305410
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs13447332
gnomAD v2: 18-58039090-G-T
MyVariant Identifiers: chr18:g.58039090G>T (hg19) chr18:g.60371857G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371857G>T , CM000680.2:g.60371857G>T GRCh38
NC_000018.9:g.58039090G>T , CM000680.1:g.58039090G>T GRCh37
NC_000018.8:g.56190070G>T NCBI36
NG_016441.1:g.5912C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.493C>A MANE Select ENSP00000299766.3:p.Arg165=
ENST00000299766.4:c.493C>A ENSP00000299766.3:p.Arg165=
NM_005912.2:c.493C>A NP_005903.2:p.Arg165=
NM_005912.3:c.493C>A MANE Select NP_005903.2:p.Arg165=
Search 100 bp 5'
Search 100 bp 3'