Canonical Allele Identifier: CA719156886
Gene: HS3ST2 HGNC NCBI

Linked Data

dbSNP Id: rs114012734
gnomAD v3: 16-22877909-G-A
gnomAD v4: 16-22877909-G-A
MyVariant Identifiers: chr16:g.22889230G>A (hg19) chr16:g.22877909G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.22877909G>A , CM000678.2:g.22877909G>A GRCh38
NC_000016.9:g.22889230G>A , CM000678.1:g.22889230G>A GRCh37
NC_000016.8:g.22796731G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261374.4:c.486-37035G>A MANE Select ENSP00000261374.3:n.486-37035G>A
ENST00000261374.3:c.486-37035G>A ENSP00000261374.3:n.486-37035G>A
ENST00000473392.1:c.*287+23128G>A ENSP00000454505.1:n.*287+23128G>A
NM_006043.1:c.486-37035G>A NP_006034.1:n.486-37035G>A
NM_006043.2:c.486-37035G>A MANE Select NP_006034.1:n.486-37035G>A
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