Canonical Allele Identifier: CA359682352

Gene: ITGA2

Linked Data

• dbSNP Id: rs1126643
• MyVariant Identifiers: chr5:g.52347369C>G (hg19) ; chr5:g.53051539C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53051539C>G , CM000667.2:g.53051539C>G	GRCh38
NC_000005.9:g.52347369C>G , CM000667.1:g.52347369C>G	GRCh37
NC_000005.8:g.52383126C>G	NCBI36
NG_008330.1:g.67214C>G
NG_008330.2:g.67214C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296585.10:c.759C>G MANE Select	ENSP00000296585.5:p.Phe253Leu
ENST00000296585.9:c.759C>G	ENSP00000296585.5:p.Phe253Leu
ENST00000503810.6:c.*103C>G	ENSP00000426489.1:n.*103C>G
ENST00000509814.5:c.759C>G	ENSP00000424397.1:p.Phe253Leu
ENST00000509960.5:c.759C>G	ENSP00000424642.1:p.Phe253Leu
ENST00000510722.1:c.759C>G	ENSP00000422145.1:p.Phe253Leu
ENST00000513685.5:c.*473C>G	ENSP00000422095.1:n.*473C>G
NM_002203.3:c.759C>G	NP_002194.2:p.Phe253Leu
NR_073103.1:n.902C>G
NR_073104.1:n.902C>G
NR_073105.1:n.902C>G
NR_073106.1:n.902C>G
NR_073107.1:n.781C>G
NM_002203.4:c.759C>G MANE Select	NP_002194.2:p.Phe253Leu
NR_073103.2:n.876C>G
NR_073104.2:n.876C>G
NR_073105.2:n.876C>G
NR_073106.2:n.876C>G
NR_073107.2:n.755C>G