Canonical Allele Identifier: CA402719000
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs1457910782
gnomAD v2: 18-58038757-A-G
gnomAD v4: 18-60371524-A-G
MyVariant Identifiers: chr18:g.58038757A>G (hg19) chr18:g.60371524A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371524A>G , CM000680.2:g.60371524A>G GRCh38
NC_000018.9:g.58038757A>G , CM000680.1:g.58038757A>G GRCh37
NC_000018.8:g.56189737A>G NCBI36
NG_016441.1:g.6245T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.826T>C MANE Select ENSP00000299766.3:p.Tyr276His
ENST00000299766.4:c.826T>C ENSP00000299766.3:p.Tyr276His
NM_005912.2:c.826T>C NP_005903.2:p.Tyr276His
NM_005912.3:c.826T>C MANE Select NP_005903.2:p.Tyr276His
Search 100 bp 5'
Search 100 bp 3'