Canonical Allele Identifier: CA288676136
Gene: HS3ST3A1 HGNC NCBI

Linked Data

dbSNP Id: rs978444643
gnomAD v3: 17-13573787-G-A
gnomAD v4: 17-13573787-G-A
MyVariant Identifiers: chr17:g.13477104G>A (hg19) chr17:g.13573787G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573787G>A , CM000679.2:g.13573787G>A GRCh38
NC_000017.10:g.13477104G>A , CM000679.1:g.13477104G>A GRCh37
NC_000017.9:g.13417829G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000284110.2:c.599+26744C>T MANE Select ENSP00000284110.1:n.599+26744C>T
ENST00000284110.1:c.599+26744C>T ENSP00000284110.1:n.599+26744C>T
NM_006042.2:c.599+26744C>T NP_006033.1:n.599+26744C>T
NM_006042.3:c.599+26744C>T MANE Select NP_006033.1:n.599+26744C>T
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