Canonical Allele Identifier: CA2638214856

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374686-CGGGGGCACCGCATA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374691_44374704del , CM000679.2:g.44374691_44374704del	GRCh38
NC_000017.10:g.42452059_42452072del , CM000679.1:g.42452059_42452072del	GRCh37
NC_000017.9:g.39807585_39807598del	NCBI36
NG_008331.1:g.19806_19819del , LRG_479:g.19806_19819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2902_2915del MANE Select	ENSP00000262407.5:p.Tyr968AlafsTer?
ENST00000648408.1:c.2333_2346del
ENST00000262407.5:c.2902_2915del	ENSP00000262407.5:p.Tyr968AlafsTer?
ENST00000587295.5:c.253+1133_253+1146del
ENST00000592462.5:n.2413_2426del
NM_000419.3:c.2902_2915del , LRG_479t1:c.2902_2915del	NP_000410.2:p.Tyr968AlafsTer?
XM_011524749.1:c.2842-230_2842-217del	XP_011523051.1:n.2842-230_2842-217del
XM_011524750.1:c.2902_2915del	XP_011523052.1:p.Tyr968AlafsTer24
NM_000419.4:c.2902_2915del	NP_000410.2:p.Tyr968AlafsTer?
NM_000419.5:c.2902_2915del MANE Select	NP_000410.2:p.Tyr968AlafsTer?