Canonical Allele Identifier: CA8980973
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs141148170
ExAC: 18:58039425 G / A
gnomAD v2: 18-58039425-G-A
gnomAD v3: 18-60372192-G-A
gnomAD v4: 18-60372192-G-A
MyVariant Identifiers: chr18:g.58039425G>A (hg19) chr18:g.60372192G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60372192G>A , CM000680.2:g.60372192G>A GRCh38
NC_000018.9:g.58039425G>A , CM000680.1:g.58039425G>A GRCh37
NC_000018.8:g.56190405G>A NCBI36
NG_016441.1:g.5577C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.158C>T MANE Select ENSP00000299766.3:p.Thr53Ile
ENST00000299766.4:c.158C>T ENSP00000299766.3:p.Thr53Ile
NM_005912.2:c.158C>T NP_005903.2:p.Thr53Ile
NM_005912.3:c.158C>T MANE Select NP_005903.2:p.Thr53Ile
Search 100 bp 5'
Search 100 bp 3'