Canonical Allele Identifier: CA2213078589
Gene: HS3ST2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.22877802T= , CM000678.2:g.22877802T= GRCh38
NC_000016.9:g.22889123T= , CM000678.1:g.22889123T= GRCh37
NC_000016.8:g.22796624T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261374.4:c.486-37142T= MANE Select ENSP00000261374.3:n.486-37142T=
ENST00000261374.3:c.486-37142T= ENSP00000261374.3:n.486-37142T=
ENST00000473392.1:c.*287+23021T= ENSP00000454505.1:n.*287+23021T=
NM_006043.1:c.486-37142T= NP_006034.1:n.486-37142T=
NM_006043.2:c.486-37142T= MANE Select NP_006034.1:n.486-37142T=
Search 100 bp 5'
Search 100 bp 3'