Canonical Allele Identifier: CA2654864578

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44886647-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886649_44886650del , CM000683.2:g.44886649_44886650del	GRCh38
NC_000021.8:g.46306564_46306565del , CM000683.1:g.46306564_46306565del	GRCh37
NC_000021.7:g.45130992_45130993del	NCBI36
NG_007270.2:g.47190_47191del , LRG_76:g.47190_47191del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1454+87_1454+88del
ENST00000302347.10:c.2319+87_2319+88del	ENSP00000303242.6:n.2319+87_2319+88del
ENST00000652462.1:c.2247+87_2247+88del MANE Select	ENSP00000498780.1:n.2247+87_2247+88del
ENST00000302347.9:c.2247+87_2247+88del	ENSP00000303242.5:n.2247+87_2247+88del
ENST00000355153.8:c.2247+87_2247+88del	ENSP00000347279.4:n.2247+87_2247+88del
ENST00000397850.6:c.2247+87_2247+88del	ENSP00000380948.2:n.2247+87_2247+88del
ENST00000397852.5:c.2247+87_2247+88del	ENSP00000380950.1:n.2247+87_2247+88del
ENST00000397854.7:c.2076+87_2076+88del	ENSP00000380952.3:n.2076+87_2076+88del
ENST00000397857.5:c.2247+87_2247+88del	ENSP00000380955.1:n.2247+87_2247+88del
ENST00000475170.5:n.1647+87_1647+88del
ENST00000479202.5:n.606+87_606+88del
ENST00000498666.5:n.4303+87_4303+88del
ENST00000523323.5:c.*2074+87_*2074+88del	ENSP00000427732.1:n.*2074+87_*2074+88del
ENST00000610622.4:c.*938+87_*938+88del	ENSP00000480700.1:n.*938+87_*938+88del
NM_000211.4:c.2247+87_2247+88del	NP_000202.3:n.2247+87_2247+88del
NM_001127491.2:c.2247+87_2247+88del	NP_001120963.2:n.2247+87_2247+88del
NM_001303238.1:c.2040+87_2040+88del	NP_001290167.1:n.2040+87_2040+88del
XM_006724001.1:c.2040+87_2040+88del	XP_006724064.1:n.2040+87_2040+88del
XM_006724001.2:c.2040+87_2040+88del	XP_006724064.1:n.2040+87_2040+88del
NM_000211.5:c.2247+87_2247+88del MANE Select	NP_000202.3:n.2247+87_2247+88del
NM_001127491.3:c.2247+87_2247+88del	NP_001120963.2:n.2247+87_2247+88del
NM_001303238.2:c.2040+87_2040+88del	NP_001290167.1:n.2040+87_2040+88del