Canonical Allele Identifier: CA91657833
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs908987424
gnomAD v3: 4-4652556-T-C
gnomAD v4: 4-4652556-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652556T>C , CM000666.2:g.4652556T>C GRCh38
NC_000004.11:g.4654283T>C , CM000666.1:g.4654283T>C GRCh37
NC_000004.10:g.4705184T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+3014T>C