Canonical Allele Identifier: CA686494392
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1412664114
MyVariant Identifiers: chr12:g.22566453T>C (hg19) chr12:g.22413519T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413519T>C , CM000674.2:g.22413519T>C GRCh38
NC_000012.11:g.22566453T>C , CM000674.1:g.22566453T>C GRCh37
NC_000012.10:g.22457720T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23357A>G
Search 100 bp 5'
Search 100 bp 3'