Canonical Allele Identifier: CA228631696
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs911025300
gnomAD v4: 11-113475581-A-G
MyVariant Identifiers: chr11:g.113346303A>G (hg19) chr11:g.113475581A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475581A>G , CM000673.2:g.113475581A>G GRCh38
NC_000011.9:g.113346303A>G , CM000673.1:g.113346303A>G GRCh37
NC_000011.8:g.112851513A>G NCBI36
NG_008841.1:g.4699T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+77T>C
XR_948024.2:n.861T>C
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