Canonical Allele Identifier: CA2213078620
Gene: HS3ST2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.22877870A= , CM000678.2:g.22877870A= GRCh38
NC_000016.9:g.22889191A= , CM000678.1:g.22889191A= GRCh37
NC_000016.8:g.22796692A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261374.4:c.486-37074A= MANE Select ENSP00000261374.3:n.486-37074A=
ENST00000261374.3:c.486-37074A= ENSP00000261374.3:n.486-37074A=
ENST00000473392.1:c.*287+23089A= ENSP00000454505.1:n.*287+23089A=
NM_006043.1:c.486-37074A= NP_006034.1:n.486-37074A=
NM_006043.2:c.486-37074A= MANE Select NP_006034.1:n.486-37074A=
Search 100 bp 5'
Search 100 bp 3'