Canonical Allele Identifier: CA184331299

Gene: SLC30A8

Linked Data

• dbSNP Id: rs966375170
• gnomAD v2: 8-118185842-C-T
• gnomAD v3: 8-117173603-C-T
• gnomAD v4: 8-117173603-C-T
• MyVariant Identifiers: chr8:g.118185842C>T (hg19) ; chr8:g.117173603C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173603C>T , CM000670.2:g.117173603C>T	GRCh38
NC_000008.10:g.118185842C>T , CM000670.1:g.118185842C>T	GRCh37
NC_000008.9:g.118255023C>T	NCBI36
NG_016991.1:g.228331C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*922C>T MANE Select	ENSP00000415011.2:n.*922C>T
ENST00000427715.2:c.*922C>T	ENSP00000407505.2:n.*922C>T
ENST00000456015.6:c.2032C>T	ENSP00000415011.2:n.2032C>T
ENST00000519688.5:c.*922C>T	ENSP00000431069.1:n.*922C>T
NM_001172811.1:c.*922C>T	NP_001166282.1:n.*922C>T
NM_001172813.1:c.*922C>T	NP_001166284.1:n.*922C>T
NM_001172814.1:c.*922C>T	NP_001166285.1:n.*922C>T
NM_001172815.1:c.*922C>T	NP_001166286.1:n.*922C>T
NM_173851.2:c.*922C>T	NP_776250.2:n.*922C>T
XM_011516881.1:c.*922C>T	XP_011515183.1:n.*922C>T
XM_011516882.1:c.*922C>T	XP_011515184.1:n.*922C>T
XR_928566.1:n.920-115G>A
XR_928567.1:n.513-115G>A
XR_928568.1:n.718-115G>A
XR_928569.1:n.761-115G>A
XR_928570.1:n.761-115G>A
NM_001172815.2:c.*922C>T	NP_001166286.1:n.*922C>T
XM_024447083.1:c.*922C>T	XP_024302851.1:n.*922C>T
XR_001746038.1:n.705-115G>A
XR_928566.2:n.863-115G>A
XR_928567.2:n.476-115G>A
XR_928568.3:n.716-115G>A
XR_928569.2:n.714-115G>A
XR_928570.2:n.714-115G>A
NM_001172811.2:c.*922C>T	NP_001166282.1:n.*922C>T
NM_001172813.2:c.*922C>T	NP_001166284.1:n.*922C>T
NM_001172814.2:c.*922C>T	NP_001166285.1:n.*922C>T
NM_173851.3:c.*922C>T MANE Select	NP_776250.2:n.*922C>T
NM_001172815.3:c.*922C>T	NP_001166286.1:n.*922C>T