Canonical Allele Identifier: CA671861638
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1428449159
gnomAD v3: 11-113475555-T-G
gnomAD v4: 11-113475555-T-G
MyVariant Identifiers: chr11:g.113346277T>G (hg19) chr11:g.113475555T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475555T>G , CM000673.2:g.113475555T>G GRCh38
NC_000011.9:g.113346277T>G , CM000673.1:g.113346277T>G GRCh37
NC_000011.8:g.112851487T>G NCBI36
NG_008841.1:g.4725A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+103A>C
XR_948024.2:n.887A>C
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