Canonical Allele Identifier: CA2261364369
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372411_44372414delinsTGAA , CM000679.2:g.44372411_44372414delinsTGAA GRCh38
NC_000017.10:g.42449779_42449782delinsTGAA , CM000679.1:g.42449779_42449782delinsTGAA GRCh37
NC_000017.9:g.39805305_39805308delinsTGAA NCBI36
NG_008331.1:g.22092_22095delinsTTCA , LRG_479:g.22092_22095delinsTTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3070_3073delinsTTCA MANE Select ENSP00000262407.5:p.Phe1024=
ENST00000648408.1:c.2384_2387delinsTTCA
ENST00000262407.5:c.3070_3073delinsTTCA ENSP00000262407.5:p.Phe1024=
ENST00000587295.5:c.263_266delinsTTCA
ENST00000588098.1:c.47_50delinsTTCA
NM_000419.3:c.3070_3073delinsTTCA , LRG_479t1:c.3070_3073delinsTTCA NP_000410.2:p.Phe1024=
XM_011524749.1:c.2968_2971delinsTTCA XP_011523051.1:p.Phe990=
XM_011524750.1:c.2953_2956delinsTTCA XP_011523052.1:p.Phe985=
NM_000419.4:c.3070_3073delinsTTCA NP_000410.2:p.Phe1024=
NM_000419.5:c.3070_3073delinsTTCA MANE Select NP_000410.2:p.Phe1024=