Canonical Allele Identifier: CA807915919
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1444019575
gnomAD v3: 5-175441525-A-T
gnomAD v4: 5-175441525-A-T
MyVariant Identifiers: chr5:g.174868528A>T (hg19) chr5:g.175441525A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441525A>T , CM000667.2:g.175441525A>T GRCh38
NC_000005.9:g.174868528A>T , CM000667.1:g.174868528A>T GRCh37
NC_000005.8:g.174801134A>T NCBI36
NG_011802.1:g.7636T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393752.3:c.*234T>A MANE Select ENSP00000377353.1:n.*234T>A
ENST00000393752.2:c.*234T>A ENSP00000377353.1:n.*234T>A
NM_000794.3:c.*234T>A NP_000785.1:n.*234T>A
NM_000794.4:c.*234T>A NP_000785.1:n.*234T>A
NM_000794.5:c.*234T>A MANE Select NP_000785.1:n.*234T>A
Search 100 bp 5'
Search 100 bp 3'