Canonical Allele Identifier: CA795370982
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1177542239
MyVariant Identifiers: chr4:g.4654215C>T (hg19) chr4:g.4652488C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652488C>T , CM000666.2:g.4652488C>T GRCh38
NC_000004.11:g.4654215C>T , CM000666.1:g.4654215C>T GRCh37
NC_000004.10:g.4705116C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+2946C>T
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Search 100 bp 3'