Canonical Allele Identifier: CA512550930

Gene: ITGB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44891898A>C , CM000683.2:g.44891898A>C	GRCh38
NC_000021.8:g.46311813A>C , CM000683.1:g.46311813A>C	GRCh37
NC_000021.7:g.45136241A>C	NCBI36
NG_007270.2:g.41941T>G , LRG_76:g.41941T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.530T>G
ENST00000302347.10:c.1395T>G	ENSP00000303242.6:p.Val465=
ENST00000652462.1:c.1323T>G MANE Select	ENSP00000498780.1:p.Val441=
ENST00000302347.9:c.1323T>G	ENSP00000303242.5:p.Val441=
ENST00000355153.8:c.1323T>G	ENSP00000347279.4:p.Val441=
ENST00000397850.6:c.1323T>G	ENSP00000380948.2:p.Val441=
ENST00000397852.5:c.1323T>G	ENSP00000380950.1:p.Val441=
ENST00000397854.7:c.1152T>G	ENSP00000380952.3:p.Val384=
ENST00000397857.5:c.1323T>G	ENSP00000380955.1:p.Val441=
ENST00000475170.5:n.723T>G
ENST00000498666.5:n.3379T>G
ENST00000523323.5:c.*1150T>G	ENSP00000427732.1:n.*1150T>G
ENST00000610622.4:c.*14T>G	ENSP00000480700.1:n.*14T>G
NM_000211.4:c.1323T>G	NP_000202.3:p.Val441=
NM_001127491.2:c.1323T>G	NP_001120963.2:p.Val441=
NM_001303238.1:c.1116T>G	NP_001290167.1:p.Val372=
XM_006724001.1:c.1116T>G	XP_006724064.1:p.Val372=
XM_006724001.2:c.1116T>G	XP_006724064.1:p.Val372=
NM_000211.5:c.1323T>G MANE Select	NP_000202.3:p.Val441=
NM_001127491.3:c.1323T>G	NP_001120963.2:p.Val441=
NM_001303238.2:c.1116T>G	NP_001290167.1:p.Val372=