Canonical Allele Identifier: CA2021550014
Gene: ST8SIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413501T= , CM000674.2:g.22413501T= GRCh38
NC_000012.11:g.22566435T= , CM000674.1:g.22566435T= GRCh37
NC_000012.10:g.22457702T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23375A=