Canonical Allele Identifier: CA228631682
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1009833837
gnomAD v2: 11-113346236-C-T
gnomAD v3: 11-113475514-C-T
gnomAD v4: 11-113475514-C-T
MyVariant Identifiers: chr11:g.113346236C>T (hg19) chr11:g.113475514C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475514C>T , CM000673.2:g.113475514C>T GRCh38
NC_000011.9:g.113346236C>T , CM000673.1:g.113346236C>T GRCh37
NC_000011.8:g.112851446C>T NCBI36
NG_008841.1:g.4766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000540600.5:n.34+144G>A
Search 100 bp 5'
Search 100 bp 3'