Canonical Allele Identifier: CA671846099

Gene: DRD2

Linked Data

• dbSNP Id: rs1314565671
• gnomAD v4: 11-113410622-G-A
• MyVariant Identifiers: chr11:g.113281344G>A (hg19) ; chr11:g.113410622G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410622G>A , CM000673.2:g.113410622G>A	GRCh38
NC_000011.9:g.113281344G>A , CM000673.1:g.113281344G>A	GRCh37
NC_000011.8:g.112786554G>A	NCBI36
NG_008841.1:g.69658C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*105C>T MANE Select	ENSP00000354859.3:n.*105C>T
ENST00000346454.7:c.*105C>T	ENSP00000278597.5:n.*105C>T
ENST00000362072.7:c.*105C>T	ENSP00000354859.3:n.*105C>T
ENST00000538967.5:c.1443C>T	ENSP00000438215.1:n.1443C>T
ENST00000542968.5:c.*105C>T	ENSP00000442172.1:n.*105C>T
ENST00000544518.5:c.*105C>T	ENSP00000441068.1:n.*105C>T
NM_000795.3:c.*105C>T	NP_000786.1:n.*105C>T
NM_016574.3:c.*105C>T	NP_057658.2:n.*105C>T
XM_017017296.2:c.*105C>T	XP_016872785.1:n.*105C>T
NM_000795.4:c.*105C>T MANE Select	NP_000786.1:n.*105C>T
NM_016574.4:c.*105C>T	NP_057658.2:n.*105C>T