Canonical Allele Identifier: CA11887338
Gene: STX18-AS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2063413

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652630T>C , CM000666.2:g.4652630T>C GRCh38
NC_000004.11:g.4654357T>C , CM000666.1:g.4654357T>C GRCh37
NC_000004.10:g.4705258T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+3088T>C