Canonical Allele Identifier: CA2638214981

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374926-ACCCCGCCCCTCCCAGAGCAAAGTGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374935_44374960del , CM000679.2:g.44374935_44374960del	GRCh38
NC_000017.10:g.42452303_42452328del , CM000679.1:g.42452303_42452328del	GRCh37
NC_000017.9:g.39807829_39807854del	NCBI36
NG_008331.1:g.19554_19579del , LRG_479:g.19554_19579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+46_2841+71del MANE Select	ENSP00000262407.5:n.2841+46_2841+71del
ENST00000648408.1:c.2272+46_2272+71del
ENST00000262407.5:c.2841+46_2841+71del	ENSP00000262407.5:n.2841+46_2841+71del
ENST00000587295.5:c.253+881_253+906del
ENST00000592462.5:n.2161_2186del
NM_000419.3:c.2841+46_2841+71del , LRG_479t1:c.2841+46_2841+71del	NP_000410.2:n.2841+46_2841+71del
XM_011524749.1:c.2841+46_2841+71del	XP_011523051.1:n.2841+46_2841+71del
XM_011524750.1:c.2841+46_2841+71del	XP_011523052.1:n.2841+46_2841+71del
NM_000419.4:c.2841+46_2841+71del	NP_000410.2:n.2841+46_2841+71del
NM_000419.5:c.2841+46_2841+71del MANE Select	NP_000410.2:n.2841+46_2841+71del