Canonical Allele Identifier: CA1022757394
Gene: ITGB2 HGNC NCBI

Linked Data

dbSNP Id: rs2083703326

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44886693_44886715del , CM000683.2:g.44886693_44886715del GRCh38
NC_000021.8:g.46306608_46306630del , CM000683.1:g.46306608_46306630del GRCh37
NC_000021.7:g.45131036_45131058del NCBI36
NG_007270.2:g.47131_47153del , LRG_76:g.47131_47153del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696946.1:n.1454+28_1454+50del
ENST00000302347.10:c.2319+28_2319+50del ENSP00000303242.6:n.2319+28_2319+50del
ENST00000652462.1:c.2247+28_2247+50del MANE Select ENSP00000498780.1:n.2247+28_2247+50del
ENST00000302347.9:c.2247+28_2247+50del ENSP00000303242.5:n.2247+28_2247+50del
ENST00000355153.8:c.2247+28_2247+50del ENSP00000347279.4:n.2247+28_2247+50del
ENST00000397850.6:c.2247+28_2247+50del ENSP00000380948.2:n.2247+28_2247+50del
ENST00000397852.5:c.2247+28_2247+50del ENSP00000380950.1:n.2247+28_2247+50del
ENST00000397854.7:c.2076+28_2076+50del ENSP00000380952.3:n.2076+28_2076+50del
ENST00000397857.5:c.2247+28_2247+50del ENSP00000380955.1:n.2247+28_2247+50del
ENST00000475170.5:n.1647+28_1647+50del
ENST00000479202.5:n.606+28_606+50del
ENST00000498666.5:n.4303+28_4303+50del
ENST00000523323.5:c.*2074+28_*2074+50del ENSP00000427732.1:n.*2074+28_*2074+50del
ENST00000610622.4:c.*938+28_*938+50del ENSP00000480700.1:n.*938+28_*938+50del
NM_000211.4:c.2247+28_2247+50del NP_000202.3:n.2247+28_2247+50del
NM_001127491.2:c.2247+28_2247+50del NP_001120963.2:n.2247+28_2247+50del
NM_001303238.1:c.2040+28_2040+50del NP_001290167.1:n.2040+28_2040+50del
XM_006724001.1:c.2040+28_2040+50del XP_006724064.1:n.2040+28_2040+50del
XM_006724001.2:c.2040+28_2040+50del XP_006724064.1:n.2040+28_2040+50del
NM_000211.5:c.2247+28_2247+50del MANE Select NP_000202.3:n.2247+28_2247+50del
NM_001127491.3:c.2247+28_2247+50del NP_001120963.2:n.2247+28_2247+50del
NM_001303238.2:c.2040+28_2040+50del NP_001290167.1:n.2040+28_2040+50del