Canonical Allele Identifier: CA2248667025
Gene: HS3ST3A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573757G= , CM000679.2:g.13573757G= GRCh38
NC_000017.10:g.13477074G= , CM000679.1:g.13477074G= GRCh37
NC_000017.9:g.13417799G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284110.2:c.599+26774C= MANE Select ENSP00000284110.1:n.599+26774C=
ENST00000284110.1:c.599+26774C= ENSP00000284110.1:n.599+26774C=
NM_006042.2:c.599+26774C= NP_006033.1:n.599+26774C=
NM_006042.3:c.599+26774C= MANE Select NP_006033.1:n.599+26774C=
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