Canonical Allele Identifier: CA807915933
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs1276322595
gnomAD v3: 5-175441538-G-A
gnomAD v4: 5-175441538-G-A
MyVariant Identifiers: chr5:g.174868541G>A (hg19) chr5:g.175441538G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441538G>A , CM000667.2:g.175441538G>A GRCh38
NC_000005.9:g.174868541G>A , CM000667.1:g.174868541G>A GRCh37
NC_000005.8:g.174801147G>A NCBI36
NG_011802.1:g.7623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393752.3:c.*221C>T MANE Select ENSP00000377353.1:n.*221C>T
ENST00000393752.2:c.*221C>T ENSP00000377353.1:n.*221C>T
NM_000794.3:c.*221C>T NP_000785.1:n.*221C>T
NM_000794.4:c.*221C>T NP_000785.1:n.*221C>T
NM_000794.5:c.*221C>T MANE Select NP_000785.1:n.*221C>T
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