Canonical Allele Identifier: CA91657704
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1035063826
MyVariant Identifiers: chr4:g.4654206A>G (hg19) chr4:g.4652479A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652479A>G , CM000666.2:g.4652479A>G GRCh38
NC_000004.11:g.4654206A>G , CM000666.1:g.4654206A>G GRCh37
NC_000004.10:g.4705107A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+2937A>G
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