Canonical Allele Identifier: CA359684307
Gene: ITGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055597T>G , CM000667.2:g.53055597T>G GRCh38
NC_000005.9:g.52351427T>G , CM000667.1:g.52351427T>G GRCh37
NC_000005.8:g.52387184T>G NCBI36
NG_008330.1:g.71272T>G
NG_008330.2:g.71272T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.839T>G MANE Select ENSP00000296585.5:p.Val280Gly
ENST00000296585.9:c.839T>G ENSP00000296585.5:p.Val280Gly
ENST00000503810.6:c.*183T>G ENSP00000426489.1:n.*183T>G
ENST00000509814.5:c.839T>G ENSP00000424397.1:p.Val280Gly
ENST00000509960.5:c.839T>G ENSP00000424642.1:p.Val280Gly
ENST00000510722.1:c.839T>G ENSP00000422145.1:p.Val280Gly
ENST00000513685.5:c.*553T>G ENSP00000422095.1:n.*553T>G
NM_002203.3:c.839T>G NP_002194.2:p.Val280Gly
NR_073103.1:n.982T>G
NR_073104.1:n.982T>G
NR_073105.1:n.982T>G
NR_073106.1:n.982T>G
NR_073107.1:n.861T>G
NM_002203.4:c.839T>G MANE Select NP_002194.2:p.Val280Gly
NR_073103.2:n.956T>G
NR_073104.2:n.956T>G
NR_073105.2:n.956T>G
NR_073106.2:n.956T>G
NR_073107.2:n.835T>G