Canonical Allele Identifier: CA601771363
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1204707098
gnomAD v2: 11-113346189-T-C
gnomAD v3: 11-113475467-T-C
gnomAD v4: 11-113475467-T-C
MyVariant Identifiers: chr11:g.113346189T>C (hg19) chr11:g.113475467T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475467T>C , CM000673.2:g.113475467T>C GRCh38
NC_000011.9:g.113346189T>C , CM000673.1:g.113346189T>C GRCh37
NC_000011.8:g.112851399T>C NCBI36
NG_008841.1:g.4813A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+191A>G
Search 100 bp 5'
Search 100 bp 3'