Canonical Allele Identifier: CA671861649
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1257123647
gnomAD v3: 11-113475582-A-T
gnomAD v4: 11-113475582-A-T
MyVariant Identifiers: chr11:g.113346304A>T (hg19) chr11:g.113475582A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475582A>T , CM000673.2:g.113475582A>T GRCh38
NC_000011.9:g.113346304A>T , CM000673.1:g.113346304A>T GRCh37
NC_000011.8:g.112851514A>T NCBI36
NG_008841.1:g.4698T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+76T>A
XR_948024.2:n.860T>A
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