Canonical Allele Identifier: CA447952059
Gene: DRD1 HGNC NCBI

Linked Data

dbSNP Id: rs155417
gnomAD v4: 5-175441837-T-A
MyVariant Identifiers: chr5:g.174868840T>A (hg19) chr5:g.175441837T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175441837T>A , CM000667.2:g.175441837T>A GRCh38
NC_000005.9:g.174868840T>A , CM000667.1:g.174868840T>A GRCh37
NC_000005.8:g.174801446T>A NCBI36
NG_011802.1:g.7324A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393752.3:c.1263A>T MANE Select ENSP00000377353.1:p.Ser421=
ENST00000393752.2:c.1263A>T ENSP00000377353.1:p.Ser421=
NM_000794.3:c.1263A>T NP_000785.1:p.Ser421=
NM_000794.4:c.1263A>T NP_000785.1:p.Ser421=
NM_000794.5:c.1263A>T MANE Select NP_000785.1:p.Ser421=
Search 100 bp 5'
Search 100 bp 3'