Canonical Allele Identifier: CA2593263710
Gene: HS3ST4 HGNC NCBI

Linked Data

dbSNP Id: rs1356879186
gnomAD v3: 16-25933255-C-T
gnomAD v4: 16-25933255-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.25933255C>T , CM000678.2:g.25933255C>T GRCh38
NC_000016.9:g.25944576C>T , CM000678.1:g.25944576C>T GRCh37
NC_000016.8:g.25852077C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331351.6:c.735-202357C>T MANE Select ENSP00000330606.5:n.735-202357C>T
ENST00000331351.5:c.735-202357C>T ENSP00000330606.5:n.735-202357C>T
ENST00000475436.1:n.176+46334C>T
NM_006040.2:c.735-202357C>T NP_006031.2:n.735-202357C>T
NM_006040.3:c.735-202357C>T MANE Select NP_006031.2:n.735-202357C>T
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