Canonical Allele Identifier: CA228636502

Gene: DRD2

Linked Data

• dbSNP Id: rs1044582172
• gnomAD v3: 11-113442701-G-A
• gnomAD v4: 11-113442701-G-A
• MyVariant Identifiers: chr11:g.113313423G>A (hg19) ; chr11:g.113442701G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442701G>A , CM000673.2:g.113442701G>A	GRCh38
NC_000011.9:g.113313423G>A , CM000673.1:g.113313423G>A	GRCh37
NC_000011.8:g.112818633G>A	NCBI36
NG_008841.1:g.37579C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-18019C>T MANE Select	ENSP00000354859.3:n.-31-18019C>T
ENST00000346454.7:c.-31-18019C>T	ENSP00000278597.5:n.-31-18019C>T
ENST00000362072.7:c.-31-18019C>T	ENSP00000354859.3:n.-31-18019C>T
ENST00000540600.5:n.35-18019C>T
ENST00000542616.1:c.-31-18019C>T	ENSP00000441474.1:n.-31-18019C>T
ENST00000543292.1:c.-32+4870C>T	ENSP00000438419.1:n.-32+4870C>T
NM_000795.3:c.-31-18019C>T	NP_000786.1:n.-31-18019C>T
NM_016574.3:c.-31-18019C>T	NP_057658.2:n.-31-18019C>T
XM_017017296.2:c.-31-18019C>T	XP_016872785.1:n.-31-18019C>T
NM_000795.4:c.-31-18019C>T MANE Select	NP_000786.1:n.-31-18019C>T
NM_016574.4:c.-31-18019C>T	NP_057658.2:n.-31-18019C>T