Canonical Allele Identifier: CA379008350
Gene: DRD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.640225C>G (hg19) chr11:g.640225C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640225C>G , CM000673.2:g.640225C>G GRCh38
NC_000011.9:g.640225C>G , CM000673.1:g.640225C>G GRCh37
NC_000011.8:g.630225C>G NCBI36
NG_021241.1:g.7921C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.976C>G MANE Select ENSP00000176183.5:p.Pro326Ala
ENST00000176183.5:c.976C>G ENSP00000176183.5:p.Pro326Ala
NM_000797.3:c.976C>G NP_000788.2:p.Pro326Ala
NM_000797.4:c.976C>G MANE Select NP_000788.2:p.Pro326Ala
Search 100 bp 5'
Search 100 bp 3'