Canonical Allele Identifier: CA11990529
Gene: DRD1 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.175443899A>G
GRCh37 chr5:g.174870902A>G
gnomAD v2:
5:174870902 A / G
gnomAD v3:
5:175443899 A / G
gnomAD v4:
chr5-175443899-A-G
Joint Max Group AF 0.9225056 (AFR)
Genomes Max Group AF 0.92247423 (AFR)
Exomes Max Group AF 0.69215467 (NFE)
dbSNP:
265981
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175443899A>G , CM000667.2:g.175443899A>G GRCh38
NC_000005.9:g.174870902A>G , CM000667.1:g.174870902A>G GRCh37
NC_000005.8:g.174803508A>G NCBI36
NG_011802.1:g.5262T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393752.3:c.-684T>C MANE Select ENSP00000377353.1:n.-684T>C
ENST00000393752.2:c.-684T>C ENSP00000377353.1:n.-684T>C
NM_000794.3:c.-684T>C NP_000785.1:n.-684T>C
NM_000794.4:c.-684T>C NP_000785.1:n.-684T>C
NM_000794.5:c.-684T>C MANE Select NP_000785.1:n.-684T>C
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