Canonical Allele Identifier: CA8980801
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs765769471
ExAC: 18:58038622 G / A
gnomAD v2: 18-58038622-G-A
gnomAD v4: 18-60371389-G-A
MyVariant Identifiers: chr18:g.58038622G>A (hg19) chr18:g.60371389G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371389G>A , CM000680.2:g.60371389G>A GRCh38
NC_000018.9:g.58038622G>A , CM000680.1:g.58038622G>A GRCh37
NC_000018.8:g.56189602G>A NCBI36
NG_016441.1:g.6380C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.961C>T MANE Select ENSP00000299766.3:p.Pro321Ser
ENST00000299766.4:c.961C>T ENSP00000299766.3:p.Pro321Ser
NM_005912.2:c.961C>T NP_005903.2:p.Pro321Ser
NM_005912.3:c.961C>T MANE Select NP_005903.2:p.Pro321Ser
Search 100 bp 5'
Search 100 bp 3'