Canonical Allele Identifier: CA228631698
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1032913901
gnomAD v4: 11-113475588-C-T
MyVariant Identifiers: chr11:g.113346310C>T (hg19) chr11:g.113475588C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475588C>T , CM000673.2:g.113475588C>T GRCh38
NC_000011.9:g.113346310C>T , CM000673.1:g.113346310C>T GRCh37
NC_000011.8:g.112851520C>T NCBI36
NG_008841.1:g.4692G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+70G>A
XR_948024.2:n.854G>A
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