Canonical Allele Identifier: CA2261364302
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372273_44372274delinsTC , CM000679.2:g.44372273_44372274delinsTC GRCh38
NC_000017.10:g.42449641_42449642delinsTC , CM000679.1:g.42449641_42449642delinsTC GRCh37
NC_000017.9:g.39805167_39805168delinsTC NCBI36
NG_008331.1:g.22232_22233delinsGA , LRG_479:g.22232_22233delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*90_*91delinsGA MANE Select ENSP00000262407.5:n.*90_*91delinsGA
ENST00000648408.1:c.2524_2525delinsGA
ENST00000262407.5:c.*90_*91delinsGA ENSP00000262407.5:n.*90_*91delinsGA
ENST00000587295.5:c.403_404delinsGA
ENST00000588098.1:c.187_188delinsGA
NM_000419.3:c.*90_*91delinsGA , LRG_479t1:c.*90_*91delinsGA NP_000410.2:n.*90_*91delinsGA
XM_011524749.1:c.*90_*91delinsGA XP_011523051.1:n.*90_*91delinsGA
XM_011524750.1:c.*90_*91delinsGA XP_011523052.1:n.*90_*91delinsGA
NM_000419.4:c.*90_*91delinsGA NP_000410.2:n.*90_*91delinsGA
NM_000419.5:c.*90_*91delinsGA MANE Select NP_000410.2:n.*90_*91delinsGA