Canonical Allele Identifier: CA2391876662
Gene: ITGB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44894994G= , CM000683.2:g.44894994G= GRCh38
NC_000021.8:g.46314909G= , CM000683.1:g.46314909G= GRCh37
NC_000021.7:g.45139337G= NCBI36
NG_007270.2:g.38845C= , LRG_76:g.38845C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302347.10:c.1132C= ENSP00000303242.6:p.His378=
ENST00000652462.1:c.1060C= MANE Select ENSP00000498780.1:p.His354=
ENST00000302347.9:c.1060C= ENSP00000303242.5:p.His354=
ENST00000355153.8:c.1060C= ENSP00000347279.4:p.His354=
ENST00000397850.6:c.1060C= ENSP00000380948.2:p.His354=
ENST00000397852.5:c.1060C= ENSP00000380950.1:p.His354=
ENST00000397854.7:c.889C= ENSP00000380952.3:p.His297=
ENST00000397857.5:c.1060C= ENSP00000380955.1:p.His354=
ENST00000498666.5:n.1203C=
ENST00000523323.5:c.*887C= ENSP00000427732.1:n.*887C=
ENST00000610622.4:c.889C= ENSP00000480700.1:p.His297=
NM_000211.4:c.1060C= NP_000202.3:p.His354=
NM_001127491.2:c.1060C= NP_001120963.2:p.His354=
NM_001303238.1:c.853C= NP_001290167.1:p.His285=
XM_006724001.1:c.853C= XP_006724064.1:p.His285=
XM_006724001.2:c.853C= XP_006724064.1:p.His285=
NM_000211.5:c.1060C= MANE Select NP_000202.3:p.His354=
NM_001127491.3:c.1060C= NP_001120963.2:p.His354=
NM_001303238.2:c.853C= NP_001290167.1:p.His285=