Canonical Allele Identifier: CA1118284781

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1818517166
• gnomAD v3: 8-117077211-T-G
• gnomAD v4: 8-117077211-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077211T>G , CM000670.2:g.117077211T>G	GRCh38
NC_000008.10:g.118089450T>G , CM000670.1:g.118089450T>G	GRCh37
NC_000008.9:g.118158631T>G	NCBI36
NG_016991.1:g.131939T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000427715.2:c.-226+37953T>G	ENSP00000407505.2:n.-226+37953T>G
ENST00000521035.5:n.295-58021T>G
ENST00000521243.5:c.-106-69608T>G	ENSP00000428545.1:n.-106-69608T>G
ENST00000524274.5:c.-106-69608T>G	ENSP00000427760.1:n.-106-69608T>G
NM_001172811.1:c.-106-69608T>G	NP_001166282.1:n.-106-69608T>G
NM_001172813.1:c.-273-58021T>G	NP_001166284.1:n.-273-58021T>G
NM_001172815.1:c.-226+37953T>G	NP_001166286.1:n.-226+37953T>G
XM_011516881.1:c.-96-58021T>G	XP_011515183.1:n.-96-58021T>G
NM_001172815.2:c.-226+37953T>G	NP_001166286.1:n.-226+37953T>G
XM_024447083.1:c.-106-69608T>G	XP_024302851.1:n.-106-69608T>G
NM_001172811.2:c.-106-69608T>G	NP_001166282.1:n.-106-69608T>G
NM_001172813.2:c.-273-58021T>G	NP_001166284.1:n.-273-58021T>G
NM_001172815.3:c.-226+37953T>G	NP_001166286.1:n.-226+37953T>G