Canonical Allele Identifier: CA472436471
Gene: DRD4 HGNC NCBI

Linked Data

gnomAD v4: 11-637580-C-T
MyVariant Identifiers: chr11:g.637580C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637580C>T , CM000673.2:g.637580C>T GRCh38
NC_000011.9:g.637580C>T , CM000673.1:g.637580C>T GRCh37
NC_000011.8:g.627580C>T NCBI36
NG_021241.1:g.5276C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.276C>T MANE Select ENSP00000176183.5:p.Val92=
ENST00000176183.5:c.276C>T ENSP00000176183.5:p.Val92=
NM_000797.3:c.276C>T NP_000788.2:p.Val92=
NM_000797.4:c.276C>T MANE Select NP_000788.2:p.Val92=
Search 100 bp 5'
Search 100 bp 3'