Canonical Allele Identifier: CA472436379
Gene: DRD4 HGNC NCBI

Linked Data

gnomAD v4: 11-637526-G-T
MyVariant Identifiers: chr11:g.637526G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637526G>T , CM000673.2:g.637526G>T GRCh38
NC_000011.9:g.637526G>T , CM000673.1:g.637526G>T GRCh37
NC_000011.8:g.627526G>T NCBI36
NG_021241.1:g.5222G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.222G>T MANE Select ENSP00000176183.5:p.Val74=
ENST00000176183.5:c.222G>T ENSP00000176183.5:p.Val74=
NM_000797.3:c.222G>T NP_000788.2:p.Val74=
NM_000797.4:c.222G>T MANE Select NP_000788.2:p.Val74=
Search 100 bp 5'
Search 100 bp 3'