Canonical Allele Identifier: CA118889270

Gene: ITGA2

Linked Data

• dbSNP Id: rs1016560654
• MyVariant Identifiers: chr5:g.52351484G>A (hg19) ; chr5:g.53055654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055654G>A , CM000667.2:g.53055654G>A	GRCh38
NC_000005.9:g.52351484G>A , CM000667.1:g.52351484G>A	GRCh37
NC_000005.8:g.52387241G>A	NCBI36
NG_008330.1:g.71329G>A
NG_008330.2:g.71329G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.896G>A MANE Select	ENSP00000296585.5:p.Cys299Tyr
ENST00000296585.9:c.896G>A	ENSP00000296585.5:p.Cys299Tyr
ENST00000503810.6:c.*240G>A	ENSP00000426489.1:n.*240G>A
ENST00000509814.5:c.896G>A	ENSP00000424397.1:p.Cys299Tyr
ENST00000509960.5:c.896G>A	ENSP00000424642.1:p.Cys299Tyr
ENST00000510722.1:c.896G>A	ENSP00000422145.1:p.Cys299Tyr
ENST00000513685.5:c.*610G>A	ENSP00000422095.1:n.*610G>A
NM_002203.3:c.896G>A	NP_002194.2:p.Cys299Tyr
NR_073103.1:n.1039G>A
NR_073104.1:n.1039G>A
NR_073105.1:n.1039G>A
NR_073106.1:n.1039G>A
NR_073107.1:n.918G>A
NM_002203.4:c.896G>A MANE Select	NP_002194.2:p.Cys299Tyr
NR_073103.2:n.1013G>A
NR_073104.2:n.1013G>A
NR_073105.2:n.1013G>A
NR_073106.2:n.1013G>A
NR_073107.2:n.892G>A