Canonical Allele Identifier: CA3262712
Gene: ITGA2 HGNC NCBI

Linked Data

dbSNP Id: rs745788030
gnomAD v2: 5-52351346-T-A
gnomAD v3: 5-53055516-T-A
gnomAD v4: 5-53055516-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055516T>A , CM000667.2:g.53055516T>A GRCh38
NC_000005.9:g.52351346T>A , CM000667.1:g.52351346T>A GRCh37
NC_000005.8:g.52387103T>A NCBI36
NG_008330.1:g.71191T>A
NG_008330.2:g.71191T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.780-22T>A MANE Select ENSP00000296585.5:n.780-22T>A
ENST00000296585.9:c.780-22T>A ENSP00000296585.5:n.780-22T>A
ENST00000503810.6:c.*124-22T>A ENSP00000426489.1:n.*124-22T>A
ENST00000509814.5:c.780-22T>A ENSP00000424397.1:n.780-22T>A
ENST00000509960.5:c.780-22T>A ENSP00000424642.1:n.780-22T>A
ENST00000510722.1:c.780-22T>A ENSP00000422145.1:n.780-22T>A
ENST00000513685.5:c.*494-22T>A ENSP00000422095.1:n.*494-22T>A
NM_002203.3:c.780-22T>A NP_002194.2:n.780-22T>A
NR_073103.1:n.923-22T>A
NR_073104.1:n.923-22T>A
NR_073105.1:n.923-22T>A
NR_073106.1:n.923-22T>A
NR_073107.1:n.802-22T>A
NM_002203.4:c.780-22T>A MANE Select NP_002194.2:n.780-22T>A
NR_073103.2:n.897-22T>A
NR_073104.2:n.897-22T>A
NR_073105.2:n.897-22T>A
NR_073106.2:n.897-22T>A
NR_073107.2:n.776-22T>A