Canonical Allele Identifier: CA14356030
Gene: HS3ST2 HGNC NCBI

Linked Data

dbSNP Id: rs66517528
gnomAD v2: 16-22889140-G-T
gnomAD v3: 16-22877819-G-T
gnomAD v4: 16-22877819-G-T
MyVariant Identifiers: chr16:g.22889140G>T (hg19) chr16:g.22877819G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.22877819G>T , CM000678.2:g.22877819G>T GRCh38
NC_000016.9:g.22889140G>T , CM000678.1:g.22889140G>T GRCh37
NC_000016.8:g.22796641G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261374.4:c.486-37125G>T MANE Select ENSP00000261374.3:n.486-37125G>T
ENST00000261374.3:c.486-37125G>T ENSP00000261374.3:n.486-37125G>T
ENST00000473392.1:c.*287+23038G>T ENSP00000454505.1:n.*287+23038G>T
NM_006043.1:c.486-37125G>T NP_006034.1:n.486-37125G>T
NM_006043.2:c.486-37125G>T MANE Select NP_006034.1:n.486-37125G>T
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