Canonical Allele Identifier: CA216943561
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs942969082
MyVariant Identifiers: chr11:g.640225C>T (hg19) chr11:g.640225C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.976C>T MANE Select ENSP00000176183.5:p.Pro326Ser
ENST00000176183.5:c.976C>T ENSP00000176183.5:p.Pro326Ser
NM_000797.3:c.976C>T NP_000788.2:p.Pro326Ser
NM_000797.4:c.976C>T MANE Select NP_000788.2:p.Pro326Ser
Search 100 bp 5'
Search 100 bp 3'