Canonical Allele Identifier: CA500263498

Gene: ITGA2B

Linked Data

• COSMIC: COSM4484657
• MyVariant Identifiers: chr17:g.42452372G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375004G>A , CM000679.2:g.44375004G>A	GRCh38
NC_000017.10:g.42452372G>A , CM000679.1:g.42452372G>A	GRCh37
NC_000017.9:g.39807898G>A	NCBI36
NG_008331.1:g.19502C>T , LRG_479:g.19502C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2835C>T MANE Select	ENSP00000262407.5:p.Leu945=
ENST00000648408.1:c.2266C>T
ENST00000262407.5:c.2835C>T	ENSP00000262407.5:p.Leu945=
ENST00000587295.5:c.253+829C>T
ENST00000592462.5:n.2109C>T
NM_000419.3:c.2835C>T , LRG_479t1:c.2835C>T	NP_000410.2:p.Leu945=
XM_011524749.1:c.2835C>T	XP_011523051.1:p.Leu945=
XM_011524750.1:c.2835C>T	XP_011523052.1:p.Leu945=
NM_000419.4:c.2835C>T	NP_000410.2:p.Leu945=
NM_000419.5:c.2835C>T MANE Select	NP_000410.2:p.Leu945=