Canonical Allele Identifier: CA234140933
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs7976082
gnomAD v2: 12-22566354-G-C
gnomAD v3: 12-22413420-G-C
gnomAD v4: 12-22413420-G-C
MyVariant Identifiers: chr12:g.22566354G>C (hg19) chr12:g.22413420G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22413420G>C , CM000674.2:g.22413420G>C GRCh38
NC_000012.11:g.22566354G>C , CM000674.1:g.22566354G>C GRCh37
NC_000012.10:g.22457621G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000536558.5:n.166+23456C>G
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