Canonical Allele Identifier: CA719156860
Gene: HS3ST2 HGNC NCBI

Linked Data

dbSNP Id: rs1440266279
gnomAD v3: 16-22877802-T-C
gnomAD v4: 16-22877802-T-C
MyVariant Identifiers: chr16:g.22889123T>C (hg19) chr16:g.22877802T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000261374.4:c.486-37142T>C MANE Select ENSP00000261374.3:n.486-37142T>C
ENST00000261374.3:c.486-37142T>C ENSP00000261374.3:n.486-37142T>C
ENST00000473392.1:c.*287+23021T>C ENSP00000454505.1:n.*287+23021T>C
NM_006043.1:c.486-37142T>C NP_006034.1:n.486-37142T>C
NM_006043.2:c.486-37142T>C MANE Select NP_006034.1:n.486-37142T>C
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