Canonical Allele Identifier: CA601771362
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1323347210
gnomAD v2: 11-113346184-G-C
gnomAD v3: 11-113475462-G-C
gnomAD v4: 11-113475462-G-C
MyVariant Identifiers: chr11:g.113346184G>C (hg19) chr11:g.113475462G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475462G>C , CM000673.2:g.113475462G>C GRCh38
NC_000011.9:g.113346184G>C , CM000673.1:g.113346184G>C GRCh37
NC_000011.8:g.112851394G>C NCBI36
NG_008841.1:g.4818C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+196C>G
Search 100 bp 5'
Search 100 bp 3'