Canonical Allele Identifier: CA2391879446
Gene: ITGB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44900281C= , CM000683.2:g.44900281C= GRCh38
NC_000021.8:g.46320196C= , CM000683.1:g.46320196C= GRCh37
NC_000021.7:g.45144624C= NCBI36
NG_007270.2:g.33558G= , LRG_76:g.33558G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302347.10:c.897+39G= ENSP00000303242.6:n.897+39G=
ENST00000652462.1:c.897+39G= MANE Select ENSP00000498780.1:n.897+39G=
ENST00000302347.9:c.897+39G= ENSP00000303242.5:n.897+39G=
ENST00000320216.10:c.870+39G= ENSP00000317697.6:n.870+39G=
ENST00000355153.8:c.897+39G= ENSP00000347279.4:n.897+39G=
ENST00000397850.6:c.897+39G= ENSP00000380948.2:n.897+39G=
ENST00000397852.5:c.897+39G= ENSP00000380950.1:n.897+39G=
ENST00000397854.7:c.726+39G= ENSP00000380952.3:n.726+39G=
ENST00000397857.5:c.897+39G= ENSP00000380955.1:n.897+39G=
ENST00000498666.5:n.1040+39G=
ENST00000523323.5:c.*724+39G= ENSP00000427732.1:n.*724+39G=
ENST00000610622.4:c.726+39G= ENSP00000480700.1:n.726+39G=
NM_000211.4:c.897+39G= NP_000202.3:n.897+39G=
NM_001127491.2:c.897+39G= NP_001120963.2:n.897+39G=
NM_001303238.1:c.690+39G= NP_001290167.1:n.690+39G=
XM_006724001.1:c.690+39G= XP_006724064.1:n.690+39G=
XM_006724001.2:c.690+39G= XP_006724064.1:n.690+39G=
NM_000211.5:c.897+39G= MANE Select NP_000202.3:n.897+39G=
NM_001127491.3:c.897+39G= NP_001120963.2:n.897+39G=
NM_001303238.2:c.690+39G= NP_001290167.1:n.690+39G=