Canonical Allele Identifier: CA2261365737

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048531842

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375396_44375397dup , CM000679.2:g.44375396_44375397dup	GRCh38
NC_000017.10:g.42452764_42452765dup , CM000679.1:g.42452764_42452765dup	GRCh37
NC_000017.9:g.39808290_39808291dup	NCBI36
NG_008331.1:g.19111_19112dup , LRG_479:g.19111_19112dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+196_2727+197dup MANE Select	ENSP00000262407.5:n.2727+196_2727+197dup
ENST00000648408.1:c.2158+196_2158+197dup
ENST00000262407.5:c.2727+196_2727+197dup	ENSP00000262407.5:n.2727+196_2727+197dup
ENST00000587295.5:c.253+438_253+439dup
ENST00000592462.5:n.1718_1719dup
NM_000419.3:c.2727+196_2727+197dup , LRG_479t1:c.2727+196_2727+197dup	NP_000410.2:n.2727+196_2727+197dup
XM_011524749.1:c.2727+196_2727+197dup	XP_011523051.1:n.2727+196_2727+197dup
XM_011524750.1:c.2727+196_2727+197dup	XP_011523052.1:n.2727+196_2727+197dup
NM_000419.4:c.2727+196_2727+197dup	NP_000410.2:n.2727+196_2727+197dup
NM_000419.5:c.2727+196_2727+197dup MANE Select	NP_000410.2:n.2727+196_2727+197dup