Canonical Allele Identifier: CA1434911465
Gene: STX18-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4652625C= , CM000666.2:g.4652625C= GRCh38
NC_000004.11:g.4654352C= , CM000666.1:g.4654352C= GRCh37
NC_000004.10:g.4705253C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037888.1:n.818+3083C=