Canonical Allele Identifier: CA228624696

Gene: DRD2

Linked Data

• dbSNP Id: rs145419243
• gnomAD v4: 11-113410627-C-A
• MyVariant Identifiers: chr11:g.113281349C>A (hg19) ; chr11:g.113410627C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410627C>A , CM000673.2:g.113410627C>A	GRCh38
NC_000011.9:g.113281349C>A , CM000673.1:g.113281349C>A	GRCh37
NC_000011.8:g.112786559C>A	NCBI36
NG_008841.1:g.69653G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*100G>T MANE Select	ENSP00000354859.3:n.*100G>T
ENST00000346454.7:c.*100G>T	ENSP00000278597.5:n.*100G>T
ENST00000362072.7:c.*100G>T	ENSP00000354859.3:n.*100G>T
ENST00000538967.5:c.1438G>T	ENSP00000438215.1:n.1438G>T
ENST00000542968.5:c.*100G>T	ENSP00000442172.1:n.*100G>T
ENST00000544518.5:c.*100G>T	ENSP00000441068.1:n.*100G>T
NM_000795.3:c.*100G>T	NP_000786.1:n.*100G>T
NM_016574.3:c.*100G>T	NP_057658.2:n.*100G>T
XM_017017296.2:c.*100G>T	XP_016872785.1:n.*100G>T
NM_000795.4:c.*100G>T MANE Select	NP_000786.1:n.*100G>T
NM_016574.4:c.*100G>T	NP_057658.2:n.*100G>T