Canonical Allele Identifier: CA294194312
Gene: ST6GALNAC2 HGNC NCBI

Linked Data

dbSNP Id: rs960946938
MyVariant Identifiers: chr17:g.74582366G>A (hg19) chr17:g.76586284G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76586284G>A , CM000679.2:g.76586284G>A GRCh38
NC_000017.10:g.74582366G>A , CM000679.1:g.74582366G>A GRCh37
NC_000017.9:g.72093961G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000588005.5:n.88+585C>T
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