Canonical Allele Identifier: CA772285663

Gene: ITGA2B

Linked Data

• dbSNP Id: rs1339423207
• MyVariant Identifiers: chr17:g.42452812_42452813insCTC (hg19) ; chr17:g.44375444_44375445insCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375449_44375451dup , CM000679.2:g.44375449_44375451dup	GRCh38
NC_000017.10:g.42452817_42452819dup , CM000679.1:g.42452817_42452819dup	GRCh37
NC_000017.9:g.39808343_39808345dup	NCBI36
NG_008331.1:g.19059_19061dup , LRG_479:g.19059_19061dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+144_2727+146dup MANE Select	ENSP00000262407.5:n.2727+144_2727+146dup
ENST00000648408.1:c.2158+144_2158+146dup
ENST00000262407.5:c.2727+144_2727+146dup	ENSP00000262407.5:n.2727+144_2727+146dup
ENST00000587295.5:c.253+386_253+388dup
ENST00000592462.5:n.1666_1668dup
NM_000419.3:c.2727+144_2727+146dup , LRG_479t1:c.2727+144_2727+146dup	NP_000410.2:n.2727+144_2727+146dup
XM_011524749.1:c.2727+144_2727+146dup	XP_011523051.1:n.2727+144_2727+146dup
XM_011524750.1:c.2727+144_2727+146dup	XP_011523052.1:n.2727+144_2727+146dup
NM_000419.4:c.2727+144_2727+146dup	NP_000410.2:n.2727+144_2727+146dup
NM_000419.5:c.2727+144_2727+146dup MANE Select	NP_000410.2:n.2727+144_2727+146dup