Canonical Allele Identifier: CA795371028
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1285735373
gnomAD v3: 4-4652607-A-G
gnomAD v4: 4-4652607-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652607A>G , CM000666.2:g.4652607A>G GRCh38
NC_000004.11:g.4654334A>G , CM000666.1:g.4654334A>G GRCh37
NC_000004.10:g.4705235A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+3065A>G