Canonical Allele Identifier: CA3262709

Gene: ITGA2

Linked Data

• dbSNP Id: rs558953467
• ExAC: 5:52351343 C / A
• gnomAD v2: 5-52351343-C-A
• gnomAD v3: 5-53055513-C-A
• gnomAD v4: 5-53055513-C-A
• MyVariant Identifiers: chr5:g.52351343C>A (hg19) ; chr5:g.52351343_52351347delinsATTTA (hg19) ; chr5:g.53055513C>A (hg38) ; chr5:g.53055513_53055517delinsATTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055513C>A , CM000667.2:g.53055513C>A	GRCh38
NC_000005.9:g.52351343C>A , CM000667.1:g.52351343C>A	GRCh37
NC_000005.8:g.52387100C>A	NCBI36
NG_008330.1:g.71188C>A
NG_008330.2:g.71188C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296585.10:c.780-25C>A MANE Select	ENSP00000296585.5:n.780-25C>A
ENST00000296585.9:c.780-25C>A	ENSP00000296585.5:n.780-25C>A
ENST00000503810.6:c.*124-25C>A	ENSP00000426489.1:n.*124-25C>A
ENST00000509814.5:c.780-25C>A	ENSP00000424397.1:n.780-25C>A
ENST00000509960.5:c.780-25C>A	ENSP00000424642.1:n.780-25C>A
ENST00000510722.1:c.780-25C>A	ENSP00000422145.1:n.780-25C>A
ENST00000513685.5:c.*494-25C>A	ENSP00000422095.1:n.*494-25C>A
NM_002203.3:c.780-25C>A	NP_002194.2:n.780-25C>A
NR_073103.1:n.923-25C>A
NR_073104.1:n.923-25C>A
NR_073105.1:n.923-25C>A
NR_073106.1:n.923-25C>A
NR_073107.1:n.802-25C>A
NM_002203.4:c.780-25C>A MANE Select	NP_002194.2:n.780-25C>A
NR_073103.2:n.897-25C>A
NR_073104.2:n.897-25C>A
NR_073105.2:n.897-25C>A
NR_073106.2:n.897-25C>A
NR_073107.2:n.776-25C>A