Canonical Allele Identifier: CA597020757
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1564913743
gnomAD v2: 11-640030-GACTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGGGTCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGACCCCTGCGGCTCCA-G
gnomAD v4: 11-640030-GACTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGGGTCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGACCCCTGCGGCTCCA-G
MyVariant Identifiers: chr11:g.640031_640174del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640038_640181del , CM000673.2:g.640038_640181del GRCh38
NC_000011.9:g.640038_640181del , CM000673.1:g.640038_640181del GRCh37
NC_000011.8:g.630038_630181del NCBI36
NG_021241.1:g.7734_7877del

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.789_932del MANE Select ENSP00000176183.5:p.Pro264_Ala311del
ENST00000176183.5:c.789_932del ENSP00000176183.5:p.Pro264_Ala311del
NM_000797.3:c.789_932del NP_000788.2:p.Pro264_Ala311del
NM_000797.4:c.789_932del MANE Select NP_000788.2:p.Pro264_Ala311del
Search 100 bp 5'
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