Canonical Allele Identifier: CA321897173
Gene: ITGB2 HGNC NCBI

Linked Data

dbSNP Id: rs1034142253

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44893108_44893118dup , CM000683.2:g.44893108_44893118dup GRCh38
NC_000021.8:g.46313023_46313033dup , CM000683.1:g.46313023_46313033dup GRCh37
NC_000021.7:g.45137451_45137461dup NCBI36
NG_007270.2:g.40731_40741dup , LRG_76:g.40731_40741dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000302347.10:c.1296+296_1296+306dup ENSP00000303242.6:n.1296+296_1296+306dup
ENST00000652462.1:c.1224+296_1224+306dup MANE Select ENSP00000498780.1:n.1224+296_1224+306dup
ENST00000302347.9:c.1224+296_1224+306dup ENSP00000303242.5:n.1224+296_1224+306dup
ENST00000355153.8:c.1224+296_1224+306dup ENSP00000347279.4:n.1224+296_1224+306dup
ENST00000397850.6:c.1224+296_1224+306dup ENSP00000380948.2:n.1224+296_1224+306dup
ENST00000397852.5:c.1224+296_1224+306dup ENSP00000380950.1:n.1224+296_1224+306dup
ENST00000397854.7:c.1053+296_1053+306dup ENSP00000380952.3:n.1053+296_1053+306dup
ENST00000397857.5:c.1224+296_1224+306dup ENSP00000380955.1:n.1224+296_1224+306dup
ENST00000475170.5:n.624+296_624+306dup
ENST00000498666.5:n.3089_3099dup
ENST00000523323.5:c.*1051+296_*1051+306dup ENSP00000427732.1:n.*1051+296_*1051+306dup
ENST00000610622.4:c.1053+296_1053+306dup ENSP00000480700.1:n.1053+296_1053+306dup
NM_000211.4:c.1224+296_1224+306dup NP_000202.3:n.1224+296_1224+306dup
NM_001127491.2:c.1224+296_1224+306dup NP_001120963.2:n.1224+296_1224+306dup
NM_001303238.1:c.1017+296_1017+306dup NP_001290167.1:n.1017+296_1017+306dup
XM_006724001.1:c.1017+296_1017+306dup XP_006724064.1:n.1017+296_1017+306dup
XM_006724001.2:c.1017+296_1017+306dup XP_006724064.1:n.1017+296_1017+306dup
NM_000211.5:c.1224+296_1224+306dup MANE Select NP_000202.3:n.1224+296_1224+306dup
NM_001127491.3:c.1224+296_1224+306dup NP_001120963.2:n.1224+296_1224+306dup
NM_001303238.2:c.1017+296_1017+306dup NP_001290167.1:n.1017+296_1017+306dup