Canonical Allele Identifier: CA2808541816

Gene: HS3ST3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.13573756T>G , CM000679.2:g.13573756T>G	GRCh38
NC_000017.10:g.13477073T>G , CM000679.1:g.13477073T>G	GRCh37
NC_000017.9:g.13417798T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284110.2:c.599+26775A>C MANE Select	ENSP00000284110.1:n.599+26775A>C
ENST00000284110.1:c.599+26775A>C	ENSP00000284110.1:n.599+26775A>C
NM_006042.2:c.599+26775A>C	NP_006033.1:n.599+26775A>C
NM_006042.3:c.599+26775A>C MANE Select	NP_006033.1:n.599+26775A>C