Canonical Allele Identifier: CA2248667044
Gene: HS3ST3A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573786C= , CM000679.2:g.13573786C= GRCh38
NC_000017.10:g.13477103C= , CM000679.1:g.13477103C= GRCh37
NC_000017.9:g.13417828C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284110.2:c.599+26745G= MANE Select ENSP00000284110.1:n.599+26745G=
ENST00000284110.1:c.599+26745G= ENSP00000284110.1:n.599+26745G=
NM_006042.2:c.599+26745G= NP_006033.1:n.599+26745G=
NM_006042.3:c.599+26745G= MANE Select NP_006033.1:n.599+26745G=
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