Canonical Allele Identifier: CA601771372
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1473267519
gnomAD v2: 11-113346202-G-C
gnomAD v3: 11-113475480-G-C
gnomAD v4: 11-113475480-G-C
MyVariant Identifiers: chr11:g.113346202G>C (hg19) chr11:g.113475480G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475480G>C , CM000673.2:g.113475480G>C GRCh38
NC_000011.9:g.113346202G>C , CM000673.1:g.113346202G>C GRCh37
NC_000011.8:g.112851412G>C NCBI36
NG_008841.1:g.4800C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000540600.5:n.34+178C>G
Search 100 bp 5'
Search 100 bp 3'