Canonical Allele Identifier: CA1118284866

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1554580921
• gnomAD v3: 8-117077427-A-C
• gnomAD v4: 8-117077427-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117077427A>C , CM000670.2:g.117077427A>C	GRCh38
NC_000008.10:g.118089666A>C , CM000670.1:g.118089666A>C	GRCh37
NC_000008.9:g.118158847A>C	NCBI36
NG_016991.1:g.132155A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427715.2:c.-226+38169A>C	ENSP00000407505.2:n.-226+38169A>C
ENST00000521035.5:n.295-57805A>C
ENST00000521243.5:c.-106-69392A>C	ENSP00000428545.1:n.-106-69392A>C
ENST00000524274.5:c.-106-69392A>C	ENSP00000427760.1:n.-106-69392A>C
NM_001172811.1:c.-106-69392A>C	NP_001166282.1:n.-106-69392A>C
NM_001172813.1:c.-273-57805A>C	NP_001166284.1:n.-273-57805A>C
NM_001172815.1:c.-226+38169A>C	NP_001166286.1:n.-226+38169A>C
XM_011516881.1:c.-96-57805A>C	XP_011515183.1:n.-96-57805A>C
NM_001172815.2:c.-226+38169A>C	NP_001166286.1:n.-226+38169A>C
XM_024447083.1:c.-106-69392A>C	XP_024302851.1:n.-106-69392A>C
NM_001172811.2:c.-106-69392A>C	NP_001166282.1:n.-106-69392A>C
NM_001172813.2:c.-273-57805A>C	NP_001166284.1:n.-273-57805A>C
NM_001172815.3:c.-226+38169A>C	NP_001166286.1:n.-226+38169A>C