Canonical Allele Identifier: CA671861672
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1279485616
MyVariant Identifiers: chr11:g.113346314C>G (hg19) chr11:g.113475592C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475592C>G , CM000673.2:g.113475592C>G GRCh38
NC_000011.9:g.113346314C>G , CM000673.1:g.113346314C>G GRCh37
NC_000011.8:g.112851524C>G NCBI36
NG_008841.1:g.4688G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000540600.5:n.34+66G>C
XR_948024.2:n.850G>C
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