Canonical Allele Identifier: CA379002863
Gene: DRD4 HGNC NCBI

Linked Data

gnomAD v4: 11-637567-T-C
MyVariant Identifiers: chr11:g.637567T>C (hg19) chr11:g.637567T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637567T>C , CM000673.2:g.637567T>C GRCh38
NC_000011.9:g.637567T>C , CM000673.1:g.637567T>C GRCh37
NC_000011.8:g.627567T>C NCBI36
NG_021241.1:g.5263T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.263T>C MANE Select ENSP00000176183.5:p.Leu88Pro
ENST00000176183.5:c.263T>C ENSP00000176183.5:p.Leu88Pro
NM_000797.3:c.263T>C NP_000788.2:p.Leu88Pro
NM_000797.4:c.263T>C MANE Select NP_000788.2:p.Leu88Pro
Search 100 bp 5'
Search 100 bp 3'