Canonical Allele Identifier: CA132784479
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs371818668
MyVariant Identifiers: chr5:g.174868543C>A (hg19) chr5:g.175441540C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441540C>A , CM000667.2:g.175441540C>A GRCh38
NC_000005.9:g.174868543C>A , CM000667.1:g.174868543C>A GRCh37
NC_000005.8:g.174801149C>A NCBI36
NG_011802.1:g.7621G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393752.3:c.*219G>T MANE Select ENSP00000377353.1:n.*219G>T
ENST00000393752.2:c.*219G>T ENSP00000377353.1:n.*219G>T
NM_000794.3:c.*219G>T NP_000785.1:n.*219G>T
NM_000794.4:c.*219G>T NP_000785.1:n.*219G>T
NM_000794.5:c.*219G>T MANE Select NP_000785.1:n.*219G>T
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Search 100 bp 3'