Canonical Allele Identifier: CA2902136
Gene: SLC30A9 HGNC NCBI

Linked Data

dbSNP Id: rs376165142
ExAC: 4:42003583 T / C
gnomAD v2: 4-42003583-T-C
gnomAD v3: 4-42001566-T-C
gnomAD v4: 4-42001566-T-C
MyVariant Identifiers: chr4:g.42003583T>C (hg19) chr4:g.42001566T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001566T>C , CM000666.2:g.42001566T>C GRCh38
NC_000004.11:g.42003583T>C , CM000666.1:g.42003583T>C GRCh37
NC_000004.10:g.41698340T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-50T>C MANE Select ENSP00000264451.6:n.110-50T>C
ENST00000264451.11:c.110-50T>C ENSP00000264451.6:n.110-50T>C
ENST00000510460.1:n.235-50T>C
ENST00000513699.5:c.110-50T>C ENSP00000423529.1:n.110-50T>C
NM_006345.3:c.110-50T>C NP_006336.3:n.110-50T>C
XM_011513620.1:c.110-50T>C XP_011511922.1:n.110-50T>C
XM_017007654.2:c.110-50T>C XP_016863143.1:n.110-50T>C
XR_001741095.2:n.260-50T>C
NM_006345.4:c.110-50T>C MANE Select NP_006336.3:n.110-50T>C
Search 100 bp 5'
Search 100 bp 3'