Canonical Allele Identifier: CA91657645
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs898861506
gnomAD v2: 4-4654187-C-T
gnomAD v3: 4-4652460-C-T
gnomAD v4: 4-4652460-C-T
MyVariant Identifiers: chr4:g.4654187C>T (hg19) chr4:g.4652460C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652460C>T , CM000666.2:g.4652460C>T GRCh38
NC_000004.11:g.4654187C>T , CM000666.1:g.4654187C>T GRCh37
NC_000004.10:g.4705088C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037888.1:n.818+2918C>T
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Search 100 bp 3'