Canonical Allele Identifier: CA2670470475
Gene: SLC30A9 HGNC NCBI

Linked Data

gnomAD v4: 4-42001561-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001561A>G , CM000666.2:g.42001561A>G GRCh38
NC_000004.11:g.42003578A>G , CM000666.1:g.42003578A>G GRCh37
NC_000004.10:g.41698335A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264451.12:c.110-55A>G MANE Select ENSP00000264451.6:n.110-55A>G
ENST00000264451.11:c.110-55A>G ENSP00000264451.6:n.110-55A>G
ENST00000510460.1:n.235-55A>G
ENST00000513699.5:c.110-55A>G ENSP00000423529.1:n.110-55A>G
NM_006345.3:c.110-55A>G NP_006336.3:n.110-55A>G
XM_011513620.1:c.110-55A>G XP_011511922.1:n.110-55A>G
XM_017007654.2:c.110-55A>G XP_016863143.1:n.110-55A>G
XR_001741095.2:n.260-55A>G
NM_006345.4:c.110-55A>G MANE Select NP_006336.3:n.110-55A>G
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