Canonical Allele Identifier: CA686494393
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1161048392
MyVariant Identifiers: chr12:g.22566455A>C (hg19) chr12:g.22413521A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413521A>C , CM000674.2:g.22413521A>C GRCh38
NC_000012.11:g.22566455A>C , CM000674.1:g.22566455A>C GRCh37
NC_000012.10:g.22457722A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23355T>G
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