Canonical Allele Identifier: CA228631662
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs973933063
MyVariant Identifiers: chr11:g.113346079G>C (hg19) chr11:g.113475357G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475357G>C , CM000673.2:g.113475357G>C GRCh38
NC_000011.9:g.113346079G>C , CM000673.1:g.113346079G>C GRCh37
NC_000011.8:g.112851289G>C NCBI36
NG_008841.1:g.4923C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-313C>G MANE Select ENSP00000354859.3:n.-313C>G
ENST00000362072.7:c.-313C>G ENSP00000354859.3:n.-313C>G
ENST00000540600.5:n.34+301C>G
NM_000795.4:c.-313C>G MANE Select NP_000786.1:n.-313C>G
NM_016574.4:c.-313C>G NP_057658.2:n.-313C>G
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