Canonical Allele Identifier: CA2673816362

Gene: ITGA2

Linked Data

• gnomAD v4: 5-53055500-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055500T>G , CM000667.2:g.53055500T>G	GRCh38
NC_000005.9:g.52351330T>G , CM000667.1:g.52351330T>G	GRCh37
NC_000005.8:g.52387087T>G	NCBI36
NG_008330.1:g.71175T>G
NG_008330.2:g.71175T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296585.10:c.780-38T>G MANE Select	ENSP00000296585.5:n.780-38T>G
ENST00000296585.9:c.780-38T>G	ENSP00000296585.5:n.780-38T>G
ENST00000503810.6:c.*124-38T>G	ENSP00000426489.1:n.*124-38T>G
ENST00000509814.5:c.780-38T>G	ENSP00000424397.1:n.780-38T>G
ENST00000509960.5:c.780-38T>G	ENSP00000424642.1:n.780-38T>G
ENST00000510722.1:c.780-38T>G	ENSP00000422145.1:n.780-38T>G
ENST00000513685.5:c.*494-38T>G	ENSP00000422095.1:n.*494-38T>G
NM_002203.3:c.780-38T>G	NP_002194.2:n.780-38T>G
NR_073103.1:n.923-38T>G
NR_073104.1:n.923-38T>G
NR_073105.1:n.923-38T>G
NR_073106.1:n.923-38T>G
NR_073107.1:n.802-38T>G
NM_002203.4:c.780-38T>G MANE Select	NP_002194.2:n.780-38T>G
NR_073103.2:n.897-38T>G
NR_073104.2:n.897-38T>G
NR_073105.2:n.897-38T>G
NR_073106.2:n.897-38T>G
NR_073107.2:n.776-38T>G