Canonical Allele Identifier: CA601777407

Gene: DRD2

Linked Data

• dbSNP Id: rs1476864196
• gnomAD v2: 11-113281400-C-A
• gnomAD v4: 11-113410678-C-A
• MyVariant Identifiers: chr11:g.113281400C>A (hg19) ; chr11:g.113410678C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410678C>A , CM000673.2:g.113410678C>A	GRCh38
NC_000011.9:g.113281400C>A , CM000673.1:g.113281400C>A	GRCh37
NC_000011.8:g.112786610C>A	NCBI36
NG_008841.1:g.69602G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*49G>T MANE Select	ENSP00000354859.3:n.*49G>T
ENST00000346454.7:c.*49G>T	ENSP00000278597.5:n.*49G>T
ENST00000362072.7:c.*49G>T	ENSP00000354859.3:n.*49G>T
ENST00000538967.5:c.1387G>T	ENSP00000438215.1:n.1387G>T
ENST00000542968.5:c.*49G>T	ENSP00000442172.1:n.*49G>T
ENST00000544518.5:c.*49G>T	ENSP00000441068.1:n.*49G>T
NM_000795.3:c.*49G>T	NP_000786.1:n.*49G>T
NM_016574.3:c.*49G>T	NP_057658.2:n.*49G>T
XM_017017296.2:c.*49G>T	XP_016872785.1:n.*49G>T
NM_000795.4:c.*49G>T MANE Select	NP_000786.1:n.*49G>T
NM_016574.4:c.*49G>T	NP_057658.2:n.*49G>T