Canonical Allele Identifier: CA91657822
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs983118067
gnomAD v3: 4-4652539-C-A
gnomAD v4: 4-4652539-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652539C>A , CM000666.2:g.4652539C>A GRCh38
NC_000004.11:g.4654266C>A , CM000666.1:g.4654266C>A GRCh37
NC_000004.10:g.4705167C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+2997C>A