Canonical Allele Identifier: CA132784493
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs939978882
gnomAD v4: 5-175441642-A-G
MyVariant Identifiers: chr5:g.174868645A>G (hg19) chr5:g.175441642A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441642A>G , CM000667.2:g.175441642A>G GRCh38
NC_000005.9:g.174868645A>G , CM000667.1:g.174868645A>G GRCh37
NC_000005.8:g.174801251A>G NCBI36
NG_011802.1:g.7519T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393752.3:c.*117T>C MANE Select ENSP00000377353.1:n.*117T>C
ENST00000393752.2:c.*117T>C ENSP00000377353.1:n.*117T>C
NM_000794.3:c.*117T>C NP_000785.1:n.*117T>C
NM_000794.4:c.*117T>C NP_000785.1:n.*117T>C
NM_000794.5:c.*117T>C MANE Select NP_000785.1:n.*117T>C
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