Canonical Allele Identifier: CA551141298
Gene: SLC30A9 HGNC NCBI

Linked Data

dbSNP Id: rs1468055438
gnomAD v2: 4-42003598-G-A
gnomAD v3: 4-42001581-G-A
gnomAD v4: 4-42001581-G-A
MyVariant Identifiers: chr4:g.42003598G>A (hg19) chr4:g.42001581G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001581G>A , CM000666.2:g.42001581G>A GRCh38
NC_000004.11:g.42003598G>A , CM000666.1:g.42003598G>A GRCh37
NC_000004.10:g.41698355G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-35G>A MANE Select ENSP00000264451.6:n.110-35G>A
ENST00000264451.11:c.110-35G>A ENSP00000264451.6:n.110-35G>A
ENST00000510460.1:n.235-35G>A
ENST00000513699.5:c.110-35G>A ENSP00000423529.1:n.110-35G>A
NM_006345.3:c.110-35G>A NP_006336.3:n.110-35G>A
XM_011513620.1:c.110-35G>A XP_011511922.1:n.110-35G>A
XM_017007654.2:c.110-35G>A XP_016863143.1:n.110-35G>A
XR_001741095.2:n.260-35G>A
NM_006345.4:c.110-35G>A MANE Select NP_006336.3:n.110-35G>A
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