Canonical Allele Identifier: CA2578333739
Gene: ITGA2 HGNC NCBI

Linked Data

gnomAD v4: 5-53055442-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055442A>T , CM000667.2:g.53055442A>T GRCh38
NC_000005.9:g.52351272A>T , CM000667.1:g.52351272A>T GRCh37
NC_000005.8:g.52387029A>T NCBI36
NG_008330.1:g.71117A>T
NG_008330.2:g.71117A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.780-96A>T MANE Select ENSP00000296585.5:n.780-96A>T
ENST00000296585.9:c.780-96A>T ENSP00000296585.5:n.780-96A>T
ENST00000503810.6:c.*124-96A>T ENSP00000426489.1:n.*124-96A>T
ENST00000509814.5:c.780-96A>T ENSP00000424397.1:n.780-96A>T
ENST00000509960.5:c.780-96A>T ENSP00000424642.1:n.780-96A>T
ENST00000510722.1:c.780-96A>T ENSP00000422145.1:n.780-96A>T
ENST00000513685.5:c.*494-96A>T ENSP00000422095.1:n.*494-96A>T
NM_002203.3:c.780-96A>T NP_002194.2:n.780-96A>T
NR_073103.1:n.923-96A>T
NR_073104.1:n.923-96A>T
NR_073105.1:n.923-96A>T
NR_073106.1:n.923-96A>T
NR_073107.1:n.802-96A>T
NM_002203.4:c.780-96A>T MANE Select NP_002194.2:n.780-96A>T
NR_073103.2:n.897-96A>T
NR_073104.2:n.897-96A>T
NR_073105.2:n.897-96A>T
NR_073106.2:n.897-96A>T
NR_073107.2:n.776-96A>T