ClinGen Allele Registry
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Canonical Allele Identifier:
CA795367502
Gene: STX18-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.4646320C>G
GRCh37
chr4:g.4648047C>G
Linked Data - NCBI & NCI
dbSNP:
870142
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.4646320C>G , CM000666.2:g.4646320C>G
GRCh38
NC_000004.11:g.4648047C>G , CM000666.1:g.4648047C>G
GRCh37
NC_000004.10:g.4698948C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_037888.1:n.516-2657C>G
Search 100 bp 5'
Search 100 bp 3'