Canonical Allele Identifier: CA279833192

Gene: HS3ST2

Linked Data

• dbSNP Id: rs1001286777
• MyVariant Identifiers: chr16:g.22889208G>T (hg19) ; chr16:g.22877887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.22877887G>T , CM000678.2:g.22877887G>T	GRCh38
NC_000016.9:g.22889208G>T , CM000678.1:g.22889208G>T	GRCh37
NC_000016.8:g.22796709G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261374.4:c.486-37057G>T MANE Select	ENSP00000261374.3:n.486-37057G>T
ENST00000261374.3:c.486-37057G>T	ENSP00000261374.3:n.486-37057G>T
ENST00000473392.1:c.*287+23106G>T	ENSP00000454505.1:n.*287+23106G>T
NM_006043.1:c.486-37057G>T	NP_006034.1:n.486-37057G>T
NM_006043.2:c.486-37057G>T MANE Select	NP_006034.1:n.486-37057G>T