Canonical Allele Identifier: CA686494389
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1397310650
MyVariant Identifiers: chr12:g.22566434G>A (hg19) chr12:g.22413500G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413500G>A , CM000674.2:g.22413500G>A GRCh38
NC_000012.11:g.22566434G>A , CM000674.1:g.22566434G>A GRCh37
NC_000012.10:g.22457701G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23376C>T
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