Canonical Allele Identifier: CA91657696
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1002860534
gnomAD v3: 4-4652474-C-T
gnomAD v4: 4-4652474-C-T
MyVariant Identifiers: chr4:g.4654201C>T (hg19) chr4:g.4652474C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652474C>T , CM000666.2:g.4652474C>T GRCh38
NC_000004.11:g.4654201C>T , CM000666.1:g.4654201C>T GRCh37
NC_000004.10:g.4705102C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+2932C>T
Search 100 bp 5'
Search 100 bp 3'