Canonical Allele Identifier: CA2248667049
Gene: HS3ST3A1 HGNC NCBI

Linked Data

dbSNP Id: rs1907878160
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573789G>C , CM000679.2:g.13573789G>C GRCh38
NC_000017.10:g.13477106G>C , CM000679.1:g.13477106G>C GRCh37
NC_000017.9:g.13417831G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000284110.2:c.599+26742C>G MANE Select ENSP00000284110.1:n.599+26742C>G
ENST00000284110.1:c.599+26742C>G ENSP00000284110.1:n.599+26742C>G
NM_006042.2:c.599+26742C>G NP_006033.1:n.599+26742C>G
NM_006042.3:c.599+26742C>G MANE Select NP_006033.1:n.599+26742C>G
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