Canonical Allele Identifier: CA2021550034
Gene: ST8SIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413522A= , CM000674.2:g.22413522A= GRCh38
NC_000012.11:g.22566456A= , CM000674.1:g.22566456A= GRCh37
NC_000012.10:g.22457723A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23354T=