Canonical Allele Identifier: CA91657747
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs138476716
gnomAD v3: 4-4652499-T-A
gnomAD v4: 4-4652499-T-A
MyVariant Identifiers: chr4:g.4654226T>A (hg19) chr4:g.4652499T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652499T>A , CM000666.2:g.4652499T>A GRCh38
NC_000004.11:g.4654226T>A , CM000666.1:g.4654226T>A GRCh37
NC_000004.10:g.4705127T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037888.1:n.818+2957T>A
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