Canonical Allele Identifier: CA379002779
Gene: DRD4 HGNC NCBI

Linked Data

gnomAD v4: 11-637546-T-G
MyVariant Identifiers: chr11:g.637546T>G (hg19) chr11:g.637546T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637546T>G , CM000673.2:g.637546T>G GRCh38
NC_000011.9:g.637546T>G , CM000673.1:g.637546T>G GRCh37
NC_000011.8:g.627546T>G NCBI36
NG_021241.1:g.5242T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.242T>G MANE Select ENSP00000176183.5:p.Leu81Arg
ENST00000176183.5:c.242T>G ENSP00000176183.5:p.Leu81Arg
NM_000797.3:c.242T>G NP_000788.2:p.Leu81Arg
NM_000797.4:c.242T>G MANE Select NP_000788.2:p.Leu81Arg
Search 100 bp 5'
Search 100 bp 3'