Canonical Allele Identifier: CA13820396
Gene: HS6ST3 HGNC NCBI

Linked Data

dbSNP Id: rs7989336
gnomAD v2: 13-97017548-G-A
gnomAD v3: 13-96365294-G-A
gnomAD v4: 13-96365294-G-A
MyVariant Identifiers: chr13:g.97017548G>A (hg19) chr13:g.96365294G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.96365294G>A , CM000675.2:g.96365294G>A GRCh38
NC_000013.10:g.97017548G>A , CM000675.1:g.97017548G>A GRCh37
NC_000013.9:g.95815549G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376705.4:c.707+273725G>A MANE Select ENSP00000365895.2:n.707+273725G>A
ENST00000376705.3:c.707+273725G>A ENSP00000365895.2:n.707+273725G>A
NM_153456.3:c.707+273725G>A NP_703157.2:n.707+273725G>A
XM_011521073.1:c.708-267781G>A XP_011519375.1:n.708-267781G>A
XM_017020543.2:c.708-122921G>A XP_016876032.1:n.708-122921G>A
NM_153456.4:c.707+273725G>A MANE Select NP_703157.2:n.707+273725G>A
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