Canonical Allele Identifier: CA379008233
Gene: DRD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.640165T>A (hg19) chr11:g.640165T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640165T>A , CM000673.2:g.640165T>A GRCh38
NC_000011.9:g.640165T>A , CM000673.1:g.640165T>A GRCh37
NC_000011.8:g.630165T>A NCBI36
NG_021241.1:g.7861T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.916T>A MANE Select ENSP00000176183.5:p.Cys306Ser
ENST00000176183.5:c.916T>A ENSP00000176183.5:p.Cys306Ser
NM_000797.3:c.916T>A NP_000788.2:p.Cys306Ser
NM_000797.4:c.916T>A MANE Select NP_000788.2:p.Cys306Ser
Search 100 bp 5'
Search 100 bp 3'