Canonical Allele Identifier: CA2391880137
Gene: ITGB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44901431G= , CM000683.2:g.44901431G= GRCh38
NC_000021.8:g.46321346G= , CM000683.1:g.46321346G= GRCh37
NC_000021.7:g.45145774G= NCBI36
NG_007270.2:g.32408C= , LRG_76:g.32408C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302347.10:c.741+61C= ENSP00000303242.6:n.741+61C=
ENST00000652462.1:c.741+61C= MANE Select ENSP00000498780.1:n.741+61C=
ENST00000302347.9:c.741+61C= ENSP00000303242.5:n.741+61C=
ENST00000320216.10:c.714+61C= ENSP00000317697.6:n.714+61C=
ENST00000355153.8:c.741+61C= ENSP00000347279.4:n.741+61C=
ENST00000397850.6:c.741+61C= ENSP00000380948.2:n.741+61C=
ENST00000397852.5:c.741+61C= ENSP00000380950.1:n.741+61C=
ENST00000397854.7:c.570+61C= ENSP00000380952.3:n.570+61C=
ENST00000397857.5:c.741+61C= ENSP00000380955.1:n.741+61C=
ENST00000498666.5:n.884+61C=
ENST00000523323.5:c.*568+61C= ENSP00000427732.1:n.*568+61C=
ENST00000610622.4:c.570+61C= ENSP00000480700.1:n.570+61C=
NM_000211.4:c.741+61C= NP_000202.3:n.741+61C=
NM_001127491.2:c.741+61C= NP_001120963.2:n.741+61C=
NM_001303238.1:c.534+61C= NP_001290167.1:n.534+61C=
XM_006724001.1:c.534+61C= XP_006724064.1:n.534+61C=
XM_006724001.2:c.534+61C= XP_006724064.1:n.534+61C=
NM_000211.5:c.741+61C= MANE Select NP_000202.3:n.741+61C=
NM_001127491.3:c.741+61C= NP_001120963.2:n.741+61C=
NM_001303238.2:c.534+61C= NP_001290167.1:n.534+61C=