Canonical Allele Identifier: CA5785890
Gene: DRD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3043135
ClinVar RCV Id: RCV003933961 RCV003988167
dbSNP Id: rs199815231
ExAC: 11:640265 G / A
gnomAD v2: 11-640265-G-A
gnomAD v3: 11-640265-G-A
gnomAD v4: 11-640265-G-A
MyVariant Identifiers: chr11:g.640265G>A (hg19) chr11:g.640265G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640265G>A , CM000673.2:g.640265G>A GRCh38
NC_000011.9:g.640265G>A , CM000673.1:g.640265G>A GRCh37
NC_000011.8:g.630265G>A NCBI36
NG_021241.1:g.7961G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1016G>A MANE Select ENSP00000176183.5:p.Gly339Asp
ENST00000176183.5:c.1016G>A ENSP00000176183.5:p.Gly339Asp
NM_000797.3:c.1016G>A NP_000788.2:p.Gly339Asp
NM_000797.4:c.1016G>A MANE Select NP_000788.2:p.Gly339Asp
Search 100 bp 5'
Search 100 bp 3'