Canonical Allele Identifier: CA184966649

Gene: SLC30A8

Linked Data

• dbSNP Id: rs902523703
• MyVariant Identifiers: chr8:g.118089540A>G (hg19) ; chr8:g.117077301A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077301A>G , CM000670.2:g.117077301A>G	GRCh38
NC_000008.10:g.118089540A>G , CM000670.1:g.118089540A>G	GRCh37
NC_000008.9:g.118158721A>G	NCBI36
NG_016991.1:g.132029A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000427715.2:c.-226+38043A>G	ENSP00000407505.2:n.-226+38043A>G
ENST00000521035.5:n.295-57931A>G
ENST00000521243.5:c.-106-69518A>G	ENSP00000428545.1:n.-106-69518A>G
ENST00000524274.5:c.-106-69518A>G	ENSP00000427760.1:n.-106-69518A>G
NM_001172811.1:c.-106-69518A>G	NP_001166282.1:n.-106-69518A>G
NM_001172813.1:c.-273-57931A>G	NP_001166284.1:n.-273-57931A>G
NM_001172815.1:c.-226+38043A>G	NP_001166286.1:n.-226+38043A>G
XM_011516881.1:c.-96-57931A>G	XP_011515183.1:n.-96-57931A>G
NM_001172815.2:c.-226+38043A>G	NP_001166286.1:n.-226+38043A>G
XM_024447083.1:c.-106-69518A>G	XP_024302851.1:n.-106-69518A>G
NM_001172811.2:c.-106-69518A>G	NP_001166282.1:n.-106-69518A>G
NM_001172813.2:c.-273-57931A>G	NP_001166284.1:n.-273-57931A>G
NM_001172815.3:c.-226+38043A>G	NP_001166286.1:n.-226+38043A>G