Canonical Allele Identifier: CA2638215337

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375315-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375316del , CM000679.2:g.44375316del	GRCh38
NC_000017.10:g.42452684del , CM000679.1:g.42452684del	GRCh37
NC_000017.9:g.39808210del	NCBI36
NG_008331.1:g.19190del , LRG_479:g.19190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2728-205del MANE Select	ENSP00000262407.5:n.2728-205del
ENST00000648408.1:c.2159-205del
ENST00000262407.5:c.2728-205del	ENSP00000262407.5:n.2728-205del
ENST00000587295.5:c.253+517del
ENST00000592462.5:n.1797del
NM_000419.3:c.2728-205del , LRG_479t1:c.2728-205del	NP_000410.2:n.2728-205del
XM_011524749.1:c.2728-205del	XP_011523051.1:n.2728-205del
XM_011524750.1:c.2728-205del	XP_011523052.1:n.2728-205del
NM_000419.4:c.2728-205del	NP_000410.2:n.2728-205del
NM_000419.5:c.2728-205del MANE Select	NP_000410.2:n.2728-205del