Canonical Allele Identifier: CA301530001
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs1029672666
MyVariant Identifiers: chr18:g.58038613C>T (hg19) chr18:g.60371380C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371380C>T , CM000680.2:g.60371380C>T GRCh38
NC_000018.9:g.58038613C>T , CM000680.1:g.58038613C>T GRCh37
NC_000018.8:g.56189593C>T NCBI36
NG_016441.1:g.6389G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.970G>A MANE Select ENSP00000299766.3:p.Gly324Ser
ENST00000299766.4:c.970G>A ENSP00000299766.3:p.Gly324Ser
NM_005912.2:c.970G>A NP_005903.2:p.Gly324Ser
NM_005912.3:c.970G>A MANE Select NP_005903.2:p.Gly324Ser
Search 100 bp 5'
Search 100 bp 3'