Canonical Allele Identifier: CA2638213395

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44372296-CTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372300_44372302del , CM000679.2:g.44372300_44372302del	GRCh38
NC_000017.10:g.42449668_42449670del , CM000679.1:g.42449668_42449670del	GRCh37
NC_000017.9:g.39805194_39805196del	NCBI36
NG_008331.1:g.22207_22209del , LRG_479:g.22207_22209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.*65_*67del MANE Select	ENSP00000262407.5:n.*65_*67del
ENST00000648408.1:c.2499_2501del
ENST00000262407.5:c.*65_*67del	ENSP00000262407.5:n.*65_*67del
ENST00000587295.5:c.378_380del
ENST00000588098.1:c.162_164del
NM_000419.3:c.*65_*67del , LRG_479t1:c.*65_*67del	NP_000410.2:n.*65_*67del
XM_011524749.1:c.*65_*67del	XP_011523051.1:n.*65_*67del
XM_011524750.1:c.*65_*67del	XP_011523052.1:n.*65_*67del
NM_000419.4:c.*65_*67del	NP_000410.2:n.*65_*67del
NM_000419.5:c.*65_*67del MANE Select	NP_000410.2:n.*65_*67del