ClinGen Allele Registry
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Canonical Allele Identifier:
CA91657878
Gene: STX18-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs879889691
MyVariant Identifiers:
chr4:g.4654358T>C (hg19)
chr4:g.4652631T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.4652631T>C , CM000666.2:g.4652631T>C
GRCh38
NC_000004.11:g.4654358T>C , CM000666.1:g.4654358T>C
GRCh37
NC_000004.10:g.4705259T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037888.1:n.818+3089T>C
Search 100 bp 5'
Search 100 bp 3'