Canonical Allele Identifier: CA2261365349

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374671_44374672delinsTC , CM000679.2:g.44374671_44374672delinsTC	GRCh38
NC_000017.10:g.42452039_42452040delinsTC , CM000679.1:g.42452039_42452040delinsTC	GRCh37
NC_000017.9:g.39807565_39807566delinsTC	NCBI36
NG_008331.1:g.19834_19835delinsGA , LRG_479:g.19834_19835delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2930_2931delinsGA MANE Select	ENSP00000262407.5:p.Arg977=
ENST00000648408.1:c.2361_2362delinsGA
ENST00000262407.5:c.2930_2931delinsGA	ENSP00000262407.5:p.Arg977=
ENST00000587295.5:c.253+1161_253+1162delinsGA
ENST00000588098.1:c.24_25delinsGA
ENST00000592462.5:n.2441_2442delinsGA
NM_000419.3:c.2930_2931delinsGA , LRG_479t1:c.2930_2931delinsGA	NP_000410.2:p.Arg977=
XM_011524749.1:c.2842-202_2842-201delinsGA	XP_011523051.1:n.2842-202_2842-201delinsGA
XM_011524750.1:c.2930_2931delinsGA	XP_011523052.1:p.Arg977=
NM_000419.4:c.2930_2931delinsGA	NP_000410.2:p.Arg977=
NM_000419.5:c.2930_2931delinsGA MANE Select	NP_000410.2:p.Arg977=