Canonical Allele Identifier: CA2214507543
Gene: HS3ST4 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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