Canonical Allele Identifier: CA91657902
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1010000738
gnomAD v3: 4-4652632-T-A
gnomAD v4: 4-4652632-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652632T>A , CM000666.2:g.4652632T>A GRCh38
NC_000004.11:g.4654359T>A , CM000666.1:g.4654359T>A GRCh37
NC_000004.10:g.4705260T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+3090T>A