Canonical Allele Identifier: CA184953966

Gene: SLC30A8

Linked Data

• dbSNP Id: rs3019885
• MyVariant Identifiers: chr8:g.118025645T>A (hg19) ; chr8:g.117013406T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117013406T>A , CM000670.2:g.117013406T>A	GRCh38
NC_000008.10:g.118025645T>A , CM000670.1:g.118025645T>A	GRCh37
NC_000008.9:g.118094826T>A	NCBI36
NG_016991.1:g.68134T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000427715.2:c.-265-25813T>A	ENSP00000407505.2:n.-265-25813T>A
ENST00000521035.5:n.294+6293T>A
ENST00000521243.5:c.-107+62287T>A	ENSP00000428545.1:n.-107+62287T>A
ENST00000524274.5:c.-107+62287T>A	ENSP00000427760.1:n.-107+62287T>A
NM_001172811.1:c.-107+62287T>A	NP_001166282.1:n.-107+62287T>A
NM_001172813.1:c.-274+6293T>A	NP_001166284.1:n.-274+6293T>A
NM_001172815.1:c.-265-25813T>A	NP_001166286.1:n.-265-25813T>A
XM_011516881.1:c.-97+62287T>A	XP_011515183.1:n.-97+62287T>A
NM_001172815.2:c.-265-25813T>A	NP_001166286.1:n.-265-25813T>A
XM_024447083.1:c.-107+62287T>A	XP_024302851.1:n.-107+62287T>A
NM_001172811.2:c.-107+62287T>A	NP_001166282.1:n.-107+62287T>A
NM_001172813.2:c.-274+6293T>A	NP_001166284.1:n.-274+6293T>A
NM_001172815.3:c.-265-25813T>A	NP_001166286.1:n.-265-25813T>A