Canonical Allele Identifier: CA2638215102

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374987-G-GCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374988_44374990dup , CM000679.2:g.44374988_44374990dup	GRCh38
NC_000017.10:g.42452356_42452358dup , CM000679.1:g.42452356_42452358dup	GRCh37
NC_000017.9:g.39807882_39807884dup	NCBI36
NG_008331.1:g.19516_19518dup , LRG_479:g.19516_19518dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+8_2841+10dup MANE Select	ENSP00000262407.5:n.2841+8_2841+10dup
ENST00000648408.1:c.2272+8_2272+10dup
ENST00000262407.5:c.2841+8_2841+10dup	ENSP00000262407.5:n.2841+8_2841+10dup
ENST00000587295.5:c.253+843_253+845dup
ENST00000592462.5:n.2123_2125dup
NM_000419.3:c.2841+8_2841+10dup , LRG_479t1:c.2841+8_2841+10dup	NP_000410.2:n.2841+8_2841+10dup
XM_011524749.1:c.2841+8_2841+10dup	XP_011523051.1:n.2841+8_2841+10dup
XM_011524750.1:c.2841+8_2841+10dup	XP_011523052.1:n.2841+8_2841+10dup
NM_000419.4:c.2841+8_2841+10dup	NP_000410.2:n.2841+8_2841+10dup
NM_000419.5:c.2841+8_2841+10dup MANE Select	NP_000410.2:n.2841+8_2841+10dup