Canonical Allele Identifier: CA2535434880
Gene: HS3ST4 HGNC NCBI

Linked Data

gnomAD v4: 16-25933252-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.25933252C>A , CM000678.2:g.25933252C>A GRCh38
NC_000016.9:g.25944573C>A , CM000678.1:g.25944573C>A GRCh37
NC_000016.8:g.25852074C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331351.6:c.735-202360C>A MANE Select ENSP00000330606.5:n.735-202360C>A
ENST00000331351.5:c.735-202360C>A ENSP00000330606.5:n.735-202360C>A
ENST00000475436.1:n.176+46331C>A
NM_006040.2:c.735-202360C>A NP_006031.2:n.735-202360C>A
NM_006040.3:c.735-202360C>A MANE Select NP_006031.2:n.735-202360C>A
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