ClinGen Allele Registry
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Canonical Allele Identifier:
CA91657902
Gene: STX18-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1010000738
gnomAD v3:
4-4652632-T-A
gnomAD v4:
4-4652632-T-A
MyVariant Identifiers:
chr4:g.4654359T>A (hg19)
chr4:g.4652632T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.4652632T>A , CM000666.2:g.4652632T>A
GRCh38
NC_000004.11:g.4654359T>A , CM000666.1:g.4654359T>A
GRCh37
NC_000004.10:g.4705260T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037888.1:n.818+3090T>A
Search 100 bp 5'
Search 100 bp 3'