Canonical Allele Identifier: CA2577624167

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44886670-CAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886674_44886676del , CM000683.2:g.44886674_44886676del	GRCh38
NC_000021.8:g.46306589_46306591del , CM000683.1:g.46306589_46306591del	GRCh37
NC_000021.7:g.45131017_45131019del	NCBI36
NG_007270.2:g.47166_47168del , LRG_76:g.47166_47168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1454+63_1454+65del
ENST00000302347.10:c.2319+63_2319+65del	ENSP00000303242.6:n.2319+63_2319+65del
ENST00000652462.1:c.2247+63_2247+65del MANE Select	ENSP00000498780.1:n.2247+63_2247+65del
ENST00000302347.9:c.2247+63_2247+65del	ENSP00000303242.5:n.2247+63_2247+65del
ENST00000355153.8:c.2247+63_2247+65del	ENSP00000347279.4:n.2247+63_2247+65del
ENST00000397850.6:c.2247+63_2247+65del	ENSP00000380948.2:n.2247+63_2247+65del
ENST00000397852.5:c.2247+63_2247+65del	ENSP00000380950.1:n.2247+63_2247+65del
ENST00000397854.7:c.2076+63_2076+65del	ENSP00000380952.3:n.2076+63_2076+65del
ENST00000397857.5:c.2247+63_2247+65del	ENSP00000380955.1:n.2247+63_2247+65del
ENST00000475170.5:n.1647+63_1647+65del
ENST00000479202.5:n.606+63_606+65del
ENST00000498666.5:n.4303+63_4303+65del
ENST00000523323.5:c.*2074+63_*2074+65del	ENSP00000427732.1:n.*2074+63_*2074+65del
ENST00000610622.4:c.*938+63_*938+65del	ENSP00000480700.1:n.*938+63_*938+65del
NM_000211.4:c.2247+63_2247+65del	NP_000202.3:n.2247+63_2247+65del
NM_001127491.2:c.2247+63_2247+65del	NP_001120963.2:n.2247+63_2247+65del
NM_001303238.1:c.2040+63_2040+65del	NP_001290167.1:n.2040+63_2040+65del
XM_006724001.1:c.2040+63_2040+65del	XP_006724064.1:n.2040+63_2040+65del
XM_006724001.2:c.2040+63_2040+65del	XP_006724064.1:n.2040+63_2040+65del
NM_000211.5:c.2247+63_2247+65del MANE Select	NP_000202.3:n.2247+63_2247+65del
NM_001127491.3:c.2247+63_2247+65del	NP_001120963.2:n.2247+63_2247+65del
NM_001303238.2:c.2040+63_2040+65del	NP_001290167.1:n.2040+63_2040+65del