Canonical Allele Identifier: CA91657878
Gene: STX18-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs879889691

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