Canonical Allele Identifier: CA2391875897
Gene: ITGB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44893469T= , CM000683.2:g.44893469T= GRCh38
NC_000021.8:g.46313384T= , CM000683.1:g.46313384T= GRCh37
NC_000021.7:g.45137812T= NCBI36
NG_007270.2:g.40370A= , LRG_76:g.40370A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302347.10:c.1231A= ENSP00000303242.6:p.Ser411=
ENST00000652462.1:c.1159A= MANE Select ENSP00000498780.1:p.Ser387=
ENST00000302347.9:c.1159A= ENSP00000303242.5:p.Ser387=
ENST00000355153.8:c.1159A= ENSP00000347279.4:p.Ser387=
ENST00000397850.6:c.1159A= ENSP00000380948.2:p.Ser387=
ENST00000397852.5:c.1159A= ENSP00000380950.1:p.Ser387=
ENST00000397854.7:c.988A= ENSP00000380952.3:p.Ser330=
ENST00000397857.5:c.1159A= ENSP00000380955.1:p.Ser387=
ENST00000475170.5:n.559A=
ENST00000498666.5:n.2728A=
ENST00000523323.5:c.*986A= ENSP00000427732.1:n.*986A=
ENST00000610622.4:c.988A= ENSP00000480700.1:p.Ser330=
NM_000211.4:c.1159A= NP_000202.3:p.Ser387=
NM_001127491.2:c.1159A= NP_001120963.2:p.Ser387=
NM_001303238.1:c.952A= NP_001290167.1:p.Ser318=
XM_006724001.1:c.952A= XP_006724064.1:p.Ser318=
XM_006724001.2:c.952A= XP_006724064.1:p.Ser318=
NM_000211.5:c.1159A= MANE Select NP_000202.3:p.Ser387=
NM_001127491.3:c.1159A= NP_001120963.2:p.Ser387=
NM_001303238.2:c.952A= NP_001290167.1:p.Ser318=