Canonical Allele Identifier: CA379008449
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1858198497
MyVariant Identifiers: chr11:g.640262C>T (hg19) chr11:g.640262C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640262C>T , CM000673.2:g.640262C>T GRCh38
NC_000011.9:g.640262C>T , CM000673.1:g.640262C>T GRCh37
NC_000011.8:g.630262C>T NCBI36
NG_021241.1:g.7958C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1013C>T MANE Select ENSP00000176183.5:p.Thr338Ile
ENST00000176183.5:c.1013C>T ENSP00000176183.5:p.Thr338Ile
NM_000797.3:c.1013C>T NP_000788.2:p.Thr338Ile
NM_000797.4:c.1013C>T MANE Select NP_000788.2:p.Thr338Ile
Search 100 bp 5'
Search 100 bp 3'