Canonical Allele Identifier: CA174852
Gene: GPR26 HGNC NCBI

Linked Data

ClinVar Variation Id: 161823
ClinVar RCV Id: RCV000149359
dbSNP Id: rs193920957
gnomAD v4: 10-123666478-C-T
MyVariant Identifiers: chr10:g.125425994C>T (hg19) chr10:g.123666478C>T (hg38)
PubMed: PMID:23265383
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123666478C>T , CM000672.2:g.123666478C>T GRCh38
NC_000010.10:g.125425994C>T , CM000672.1:g.125425994C>T GRCh37
NC_000010.9:g.125415984C>T NCBI36
NG_051571.1:g.5124C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284674.2:c.71C>T MANE Select ENSP00000284674.1:p.Ala24Val
ENST00000284674.1:c.71C>T ENSP00000284674.1:p.Ala24Val
NM_153442.3:c.71C>T NP_703143.1:p.Ala24Val
NM_153442.4:c.71C>T MANE Select NP_703143.1:p.Ala24Val
Search 100 bp 5'
Search 100 bp 3'