Canonical Allele Identifier: CA472436453
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs749224739
gnomAD v4: 11-637571-G-T
MyVariant Identifiers: chr11:g.637571G>T (hg19) chr11:g.637571G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637571G>T , CM000673.2:g.637571G>T GRCh38
NC_000011.9:g.637571G>T , CM000673.1:g.637571G>T GRCh37
NC_000011.8:g.627571G>T NCBI36
NG_021241.1:g.5267G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.267G>T MANE Select ENSP00000176183.5:p.Pro89=
ENST00000176183.5:c.267G>T ENSP00000176183.5:p.Pro89=
NM_000797.3:c.267G>T NP_000788.2:p.Pro89=
NM_000797.4:c.267G>T MANE Select NP_000788.2:p.Pro89=
Search 100 bp 5'
Search 100 bp 3'