Canonical Allele Identifier: CA551141296

Gene: SLC30A9

Linked Data

• dbSNP Id: rs1409776534
• gnomAD v2: 4-42003572-G-T
• gnomAD v3: 4-42001555-G-T
• gnomAD v4: 4-42001555-G-T
• MyVariant Identifiers: chr4:g.42003572G>T (hg19) ; chr4:g.42001555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42001555G>T , CM000666.2:g.42001555G>T	GRCh38
NC_000004.11:g.42003572G>T , CM000666.1:g.42003572G>T	GRCh37
NC_000004.10:g.41698329G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264451.12:c.110-61G>T MANE Select	ENSP00000264451.6:n.110-61G>T
ENST00000264451.11:c.110-61G>T	ENSP00000264451.6:n.110-61G>T
ENST00000510460.1:n.235-61G>T
ENST00000513699.5:c.110-61G>T	ENSP00000423529.1:n.110-61G>T
NM_006345.3:c.110-61G>T	NP_006336.3:n.110-61G>T
XM_011513620.1:c.110-61G>T	XP_011511922.1:n.110-61G>T
XM_017007654.2:c.110-61G>T	XP_016863143.1:n.110-61G>T
XR_001741095.2:n.260-61G>T
NM_006345.4:c.110-61G>T MANE Select	NP_006336.3:n.110-61G>T