Canonical Allele Identifier: CA2638215252

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375230-C-CCTGATGGGAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375231_44375232insTGATGGGAAGGC , CM000679.2:g.44375231_44375232insTGATGGGAAGGC	GRCh38
NC_000017.10:g.42452599_42452600insTGATGGGAAGGC , CM000679.1:g.42452599_42452600insTGATGGGAAGGC	GRCh37
NC_000017.9:g.39808125_39808126insTGATGGGAAGGC	NCBI36
NG_008331.1:g.19275_19276insCCTTCCCATCAG , LRG_479:g.19275_19276insCCTTCCCATCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2728-120_2728-119insCCTTCCCATCAG MANE Select	ENSP00000262407.5:n.2728-120_2728-119insCCTTCCCATCAG
ENST00000648408.1:c.2159-120_2159-119insCCTTCCCATCAG
ENST00000262407.5:c.2728-120_2728-119insCCTTCCCATCAG	ENSP00000262407.5:n.2728-120_2728-119insCCTTCCCATCAG
ENST00000587295.5:c.253+602_253+603insCCTTCCCATCAG
ENST00000592462.5:n.1882_1883insCCTTCCCATCAG
NM_000419.3:c.2728-120_2728-119insCCTTCCCATCAG , LRG_479t1:c.2728-120_2728-119insCCTTCCCATCAG	NP_000410.2:n.2728-120_2728-119insCCTTCCCATCAG
XM_011524749.1:c.2728-120_2728-119insCCTTCCCATCAG	XP_011523051.1:n.2728-120_2728-119insCCTTCCCATCAG
XM_011524750.1:c.2728-120_2728-119insCCTTCCCATCAG	XP_011523052.1:n.2728-120_2728-119insCCTTCCCATCAG
NM_000419.4:c.2728-120_2728-119insCCTTCCCATCAG	NP_000410.2:n.2728-120_2728-119insCCTTCCCATCAG
NM_000419.5:c.2728-120_2728-119insCCTTCCCATCAG MANE Select	NP_000410.2:n.2728-120_2728-119insCCTTCCCATCAG