Canonical Allele Identifier: CA2578333745
Gene: ITGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055510A>G , CM000667.2:g.53055510A>G GRCh38
NC_000005.9:g.52351340A>G , CM000667.1:g.52351340A>G GRCh37
NC_000005.8:g.52387097A>G NCBI36
NG_008330.1:g.71185A>G
NG_008330.2:g.71185A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296585.10:c.780-28A>G MANE Select ENSP00000296585.5:n.780-28A>G
ENST00000296585.9:c.780-28A>G ENSP00000296585.5:n.780-28A>G
ENST00000503810.6:c.*124-28A>G ENSP00000426489.1:n.*124-28A>G
ENST00000509814.5:c.780-28A>G ENSP00000424397.1:n.780-28A>G
ENST00000509960.5:c.780-28A>G ENSP00000424642.1:n.780-28A>G
ENST00000510722.1:c.780-28A>G ENSP00000422145.1:n.780-28A>G
ENST00000513685.5:c.*494-28A>G ENSP00000422095.1:n.*494-28A>G
NM_002203.3:c.780-28A>G NP_002194.2:n.780-28A>G
NR_073103.1:n.923-28A>G
NR_073104.1:n.923-28A>G
NR_073105.1:n.923-28A>G
NR_073106.1:n.923-28A>G
NR_073107.1:n.802-28A>G
NM_002203.4:c.780-28A>G MANE Select NP_002194.2:n.780-28A>G
NR_073103.2:n.897-28A>G
NR_073104.2:n.897-28A>G
NR_073105.2:n.897-28A>G
NR_073106.2:n.897-28A>G
NR_073107.2:n.776-28A>G