Canonical Allele Identifier: CA95845426
Gene: SLC30A9 HGNC NCBI

Linked Data

dbSNP Id: rs1046969465
gnomAD v2: 4-42003582-A-G
gnomAD v3: 4-42001565-A-G
gnomAD v4: 4-42001565-A-G
MyVariant Identifiers: chr4:g.42003582A>G (hg19) chr4:g.42001565A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001565A>G , CM000666.2:g.42001565A>G GRCh38
NC_000004.11:g.42003582A>G , CM000666.1:g.42003582A>G GRCh37
NC_000004.10:g.41698339A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264451.12:c.110-51A>G MANE Select ENSP00000264451.6:n.110-51A>G
ENST00000264451.11:c.110-51A>G ENSP00000264451.6:n.110-51A>G
ENST00000510460.1:n.235-51A>G
ENST00000513699.5:c.110-51A>G ENSP00000423529.1:n.110-51A>G
NM_006345.3:c.110-51A>G NP_006336.3:n.110-51A>G
XM_011513620.1:c.110-51A>G XP_011511922.1:n.110-51A>G
XM_017007654.2:c.110-51A>G XP_016863143.1:n.110-51A>G
XR_001741095.2:n.260-51A>G
NM_006345.4:c.110-51A>G MANE Select NP_006336.3:n.110-51A>G
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