Canonical Allele Identifier: CA2391880202
Gene: ITGB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44901547T= , CM000683.2:g.44901547T= GRCh38
NC_000021.8:g.46321462T= , CM000683.1:g.46321462T= GRCh37
NC_000021.7:g.45145890T= NCBI36
NG_007270.2:g.32292A= , LRG_76:g.32292A=

Transcript Alleles

HGVS Amino-acid change
ENST00000302347.10:c.686A= ENSP00000303242.6:p.Asn229=
ENST00000652462.1:c.686A= MANE Select ENSP00000498780.1:p.Asn229=
ENST00000302347.9:c.686A= ENSP00000303242.5:p.Asn229=
ENST00000320216.10:c.659A= ENSP00000317697.6:p.Asn220=
ENST00000355153.8:c.686A= ENSP00000347279.4:p.Asn229=
ENST00000397850.6:c.686A= ENSP00000380948.2:p.Asn229=
ENST00000397852.5:c.686A= ENSP00000380950.1:p.Asn229=
ENST00000397854.7:c.515A= ENSP00000380952.3:p.Asn172=
ENST00000397857.5:c.686A= ENSP00000380955.1:p.Asn229=
ENST00000498666.5:n.829A=
ENST00000523323.5:c.*513A= ENSP00000427732.1:n.*513A=
ENST00000610622.4:c.515A= ENSP00000480700.1:p.Asn172=
NM_000211.4:c.686A= NP_000202.3:p.Asn229=
NM_001127491.2:c.686A= NP_001120963.2:p.Asn229=
NM_001303238.1:c.479A= NP_001290167.1:p.Asn160=
XM_006724001.1:c.479A= XP_006724064.1:p.Asn160=
XM_006724001.2:c.479A= XP_006724064.1:p.Asn160=
NM_000211.5:c.686A= MANE Select NP_000202.3:p.Asn229=
NM_001127491.3:c.686A= NP_001120963.2:p.Asn229=
NM_001303238.2:c.479A= NP_001290167.1:p.Asn160=