Canonical Allele Identifier: CA2638214870

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374792-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374794_44374796del , CM000679.2:g.44374794_44374796del	GRCh38
NC_000017.10:g.42452162_42452164del , CM000679.1:g.42452162_42452164del	GRCh37
NC_000017.9:g.39807688_39807690del	NCBI36
NG_008331.1:g.19711_19713del , LRG_479:g.19711_19713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-35_2842-33del MANE Select	ENSP00000262407.5:n.2842-35_2842-33del
ENST00000648408.1:c.2273-35_2273-33del
ENST00000262407.5:c.2842-35_2842-33del	ENSP00000262407.5:n.2842-35_2842-33del
ENST00000587295.5:c.253+1038_253+1040del
ENST00000592462.5:n.2318_2320del
NM_000419.3:c.2842-35_2842-33del , LRG_479t1:c.2842-35_2842-33del	NP_000410.2:n.2842-35_2842-33del
XM_011524749.1:c.2841+203_2841+205del	XP_011523051.1:n.2841+203_2841+205del
XM_011524750.1:c.2842-35_2842-33del	XP_011523052.1:n.2842-35_2842-33del
NM_000419.4:c.2842-35_2842-33del	NP_000410.2:n.2842-35_2842-33del
NM_000419.5:c.2842-35_2842-33del MANE Select	NP_000410.2:n.2842-35_2842-33del