Canonical Allele Identifier: CA228631701
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs942513804
MyVariant Identifiers: chr11:g.113475591T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475591T>C , CM000673.2:g.113475591T>C GRCh38
NC_000011.9:g.113346313T>C , CM000673.1:g.113346313T>C GRCh37
NC_000011.8:g.112851523T>C NCBI36
NG_008841.1:g.4689A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000540600.5:n.34+67A>G
XR_948024.2:n.851A>G