Canonical Allele Identifier: CA234140934
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs773155060
MyVariant Identifiers: chr12:g.22566356T>C (hg19) chr12:g.22413422T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413422T>C , CM000674.2:g.22413422T>C GRCh38
NC_000012.11:g.22566356T>C , CM000674.1:g.22566356T>C GRCh37
NC_000012.10:g.22457623T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23454A>G
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