Canonical Allele Identifier: CA288676133
Gene: HS3ST3A1 HGNC NCBI

Linked Data

dbSNP Id: rs561154942
MyVariant Identifiers: chr17:g.13477097C>T (hg19) chr17:g.13573780C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573780C>T , CM000679.2:g.13573780C>T GRCh38
NC_000017.10:g.13477097C>T , CM000679.1:g.13477097C>T GRCh37
NC_000017.9:g.13417822C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284110.2:c.599+26751G>A MANE Select ENSP00000284110.1:n.599+26751G>A
ENST00000284110.1:c.599+26751G>A ENSP00000284110.1:n.599+26751G>A
NM_006042.2:c.599+26751G>A NP_006033.1:n.599+26751G>A
NM_006042.3:c.599+26751G>A MANE Select NP_006033.1:n.599+26751G>A
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