Canonical Allele Identifier: CA2213078585

Gene: HS3ST2

Linked Data

• dbSNP Id: rs1901939401

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.22877795T>C , CM000678.2:g.22877795T>C	GRCh38
NC_000016.9:g.22889116T>C , CM000678.1:g.22889116T>C	GRCh37
NC_000016.8:g.22796617T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261374.4:c.486-37149T>C MANE Select	ENSP00000261374.3:n.486-37149T>C
ENST00000261374.3:c.486-37149T>C	ENSP00000261374.3:n.486-37149T>C
ENST00000473392.1:c.*287+23014T>C	ENSP00000454505.1:n.*287+23014T>C
NM_006043.1:c.486-37149T>C	NP_006034.1:n.486-37149T>C
NM_006043.2:c.486-37149T>C MANE Select	NP_006034.1:n.486-37149T>C