Canonical Allele Identifier: CA807915887
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1331643462
gnomAD v4: 5-175441468-C-G
MyVariant Identifiers: chr5:g.174868471C>G (hg19) chr5:g.175441468C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441468C>G , CM000667.2:g.175441468C>G GRCh38
NC_000005.9:g.174868471C>G , CM000667.1:g.174868471C>G GRCh37
NC_000005.8:g.174801077C>G NCBI36
NG_011802.1:g.7693G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393752.3:c.*291G>C MANE Select ENSP00000377353.1:n.*291G>C
ENST00000393752.2:c.*291G>C ENSP00000377353.1:n.*291G>C
NM_000794.3:c.*291G>C NP_000785.1:n.*291G>C
NM_000794.4:c.*291G>C NP_000785.1:n.*291G>C
NM_000794.5:c.*291G>C MANE Select NP_000785.1:n.*291G>C
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