Canonical Allele Identifier: CA846188163

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1473801986
• MyVariant Identifiers: chr8:g.118089557T>C (hg19) ; chr8:g.117077318T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077318T>C , CM000670.2:g.117077318T>C	GRCh38
NC_000008.10:g.118089557T>C , CM000670.1:g.118089557T>C	GRCh37
NC_000008.9:g.118158738T>C	NCBI36
NG_016991.1:g.132046T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000427715.2:c.-226+38060T>C	ENSP00000407505.2:n.-226+38060T>C
ENST00000521035.5:n.295-57914T>C
ENST00000521243.5:c.-106-69501T>C	ENSP00000428545.1:n.-106-69501T>C
ENST00000524274.5:c.-106-69501T>C	ENSP00000427760.1:n.-106-69501T>C
NM_001172811.1:c.-106-69501T>C	NP_001166282.1:n.-106-69501T>C
NM_001172813.1:c.-273-57914T>C	NP_001166284.1:n.-273-57914T>C
NM_001172815.1:c.-226+38060T>C	NP_001166286.1:n.-226+38060T>C
XM_011516881.1:c.-96-57914T>C	XP_011515183.1:n.-96-57914T>C
NM_001172815.2:c.-226+38060T>C	NP_001166286.1:n.-226+38060T>C
XM_024447083.1:c.-106-69501T>C	XP_024302851.1:n.-106-69501T>C
NM_001172811.2:c.-106-69501T>C	NP_001166282.1:n.-106-69501T>C
NM_001172813.2:c.-273-57914T>C	NP_001166284.1:n.-273-57914T>C
NM_001172815.3:c.-226+38060T>C	NP_001166286.1:n.-226+38060T>C