Canonical Allele Identifier: CA301530034
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs1016862
MyVariant Identifiers: chr18:g.58039077A>C (hg19) chr18:g.60371844A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371844A>C , CM000680.2:g.60371844A>C GRCh38
NC_000018.9:g.58039077A>C , CM000680.1:g.58039077A>C GRCh37
NC_000018.8:g.56190057A>C NCBI36
NG_016441.1:g.5925T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.506T>G MANE Select ENSP00000299766.3:p.Ile169Ser
ENST00000299766.4:c.506T>G ENSP00000299766.3:p.Ile169Ser
NM_005912.2:c.506T>G NP_005903.2:p.Ile169Ser
NM_005912.3:c.506T>G MANE Select NP_005903.2:p.Ile169Ser
Search 100 bp 5'
Search 100 bp 3'