Canonical Allele Identifier: CA321897506
Gene: ITGB2 HGNC NCBI

Linked Data

dbSNP Id: rs904201980

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44893438C>G , CM000683.2:g.44893438C>G GRCh38
NC_000021.8:g.46313353C>G , CM000683.1:g.46313353C>G GRCh37
NC_000021.7:g.45137781C>G NCBI36
NG_007270.2:g.40401G>C , LRG_76:g.40401G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302347.10:c.1262G>C ENSP00000303242.6:p.Arg421Thr
ENST00000652462.1:c.1190G>C MANE Select ENSP00000498780.1:p.Arg397Thr
ENST00000302347.9:c.1190G>C ENSP00000303242.5:p.Arg397Thr
ENST00000355153.8:c.1190G>C ENSP00000347279.4:p.Arg397Thr
ENST00000397850.6:c.1190G>C ENSP00000380948.2:p.Arg397Thr
ENST00000397852.5:c.1190G>C ENSP00000380950.1:p.Arg397Thr
ENST00000397854.7:c.1019G>C ENSP00000380952.3:p.Arg340Thr
ENST00000397857.5:c.1190G>C ENSP00000380955.1:p.Arg397Thr
ENST00000475170.5:n.590G>C
ENST00000498666.5:n.2759G>C
ENST00000523323.5:c.*1017G>C ENSP00000427732.1:n.*1017G>C
ENST00000610622.4:c.1019G>C ENSP00000480700.1:p.Arg340Thr
NM_000211.4:c.1190G>C NP_000202.3:p.Arg397Thr
NM_001127491.2:c.1190G>C NP_001120963.2:p.Arg397Thr
NM_001303238.1:c.983G>C NP_001290167.1:p.Arg328Thr
XM_006724001.1:c.983G>C XP_006724064.1:p.Arg328Thr
XM_006724001.2:c.983G>C XP_006724064.1:p.Arg328Thr
NM_000211.5:c.1190G>C MANE Select NP_000202.3:p.Arg397Thr
NM_001127491.3:c.1190G>C NP_001120963.2:p.Arg397Thr
NM_001303238.2:c.983G>C NP_001290167.1:p.Arg328Thr