Canonical Allele Identifier: CA846175212
Gene: SLC30A8 HGNC NCBI

Linked Data

dbSNP Id: rs1244793035

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117151054C>T , CM000670.2:g.117151054C>T GRCh38
NC_000008.10:g.118163293C>T , CM000670.1:g.118163293C>T GRCh37
NC_000008.9:g.118232474C>T NCBI36
NG_016991.1:g.205782C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000456015.7:c.272-1890C>T MANE Select ENSP00000415011.2:n.272-1890C>T
ENST00000427715.2:c.125-1890C>T ENSP00000407505.2:n.125-1890C>T
ENST00000456015.6:c.272-1890C>T ENSP00000415011.2:n.272-1890C>T
ENST00000518521.5:c.125-1890C>T ENSP00000485566.1:n.125-1890C>T
ENST00000519688.5:c.125-1890C>T ENSP00000431069.1:n.125-1890C>T
ENST00000521243.5:c.125-1890C>T ENSP00000428545.1:n.125-1890C>T
ENST00000524274.5:c.125-1890C>T ENSP00000427760.1:n.125-1890C>T
NM_001172811.1:c.125-1890C>T NP_001166282.1:n.125-1890C>T
NM_001172813.1:c.125-1890C>T NP_001166284.1:n.125-1890C>T
NM_001172814.1:c.125-1890C>T NP_001166285.1:n.125-1890C>T
NM_001172815.1:c.125-1890C>T NP_001166286.1:n.125-1890C>T
NM_173851.2:c.272-1890C>T NP_776250.2:n.272-1890C>T
XM_011516881.1:c.272-1890C>T XP_011515183.1:n.272-1890C>T
XM_011516882.1:c.125-1890C>T XP_011515184.1:n.125-1890C>T
XR_928569.1:n.1020+21561G>A
XR_928570.1:n.1020+21561G>A
NM_001172815.2:c.125-1890C>T NP_001166286.1:n.125-1890C>T
XM_024447083.1:c.125-1890C>T XP_024302851.1:n.125-1890C>T
XR_928569.2:n.973+21561G>A
XR_928570.2:n.973+21561G>A
NM_001172811.2:c.125-1890C>T NP_001166282.1:n.125-1890C>T
NM_001172813.2:c.125-1890C>T NP_001166284.1:n.125-1890C>T
NM_001172814.2:c.125-1890C>T NP_001166285.1:n.125-1890C>T
NM_173851.3:c.272-1890C>T MANE Select NP_776250.2:n.272-1890C>T
NM_001172815.3:c.125-1890C>T NP_001166286.1:n.125-1890C>T