Canonical Allele Identifier: CA184966630

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1003703133
• MyVariant Identifiers: chr8:g.118089364C>T (hg19) ; chr8:g.117077125C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077125C>T , CM000670.2:g.117077125C>T	GRCh38
NC_000008.10:g.118089364C>T , CM000670.1:g.118089364C>T	GRCh37
NC_000008.9:g.118158545C>T	NCBI36
NG_016991.1:g.131853C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+37867C>T	ENSP00000407505.2:n.-226+37867C>T
ENST00000521035.5:n.295-58107C>T
ENST00000521243.5:c.-106-69694C>T	ENSP00000428545.1:n.-106-69694C>T
ENST00000524274.5:c.-106-69694C>T	ENSP00000427760.1:n.-106-69694C>T
NM_001172811.1:c.-106-69694C>T	NP_001166282.1:n.-106-69694C>T
NM_001172813.1:c.-273-58107C>T	NP_001166284.1:n.-273-58107C>T
NM_001172815.1:c.-226+37867C>T	NP_001166286.1:n.-226+37867C>T
XM_011516881.1:c.-96-58107C>T	XP_011515183.1:n.-96-58107C>T
NM_001172815.2:c.-226+37867C>T	NP_001166286.1:n.-226+37867C>T
XM_024447083.1:c.-106-69694C>T	XP_024302851.1:n.-106-69694C>T
NM_001172811.2:c.-106-69694C>T	NP_001166282.1:n.-106-69694C>T
NM_001172813.2:c.-273-58107C>T	NP_001166284.1:n.-273-58107C>T
NM_001172815.3:c.-226+37867C>T	NP_001166286.1:n.-226+37867C>T