Canonical Allele Identifier: CA2001188673
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1951474181
gnomAD v4: 11-113475366-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475366G>T , CM000673.2:g.113475366G>T GRCh38
NC_000011.9:g.113346088G>T , CM000673.1:g.113346088G>T GRCh37
NC_000011.8:g.112851298G>T NCBI36
NG_008841.1:g.4914C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-322C>A MANE Select ENSP00000354859.3:n.-322C>A
ENST00000362072.7:c.-322C>A ENSP00000354859.3:n.-322C>A
ENST00000540600.5:n.34+292C>A
NM_000795.4:c.-322C>A MANE Select NP_000786.1:n.-322C>A
NM_016574.4:c.-322C>A NP_057658.2:n.-322C>A
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