Canonical Allele Identifier: CA2654864641

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44886962-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886962C>G , CM000683.2:g.44886962C>G	GRCh38
NC_000021.8:g.46306877C>G , CM000683.1:g.46306877C>G	GRCh37
NC_000021.7:g.45131305C>G	NCBI36
NG_007270.2:g.46877G>C , LRG_76:g.46877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1288-60G>C
ENST00000302347.10:c.2153-60G>C	ENSP00000303242.6:n.2153-60G>C
ENST00000652462.1:c.2081-60G>C MANE Select	ENSP00000498780.1:n.2081-60G>C
ENST00000302347.9:c.2081-60G>C	ENSP00000303242.5:n.2081-60G>C
ENST00000355153.8:c.2081-60G>C	ENSP00000347279.4:n.2081-60G>C
ENST00000397850.6:c.2081-60G>C	ENSP00000380948.2:n.2081-60G>C
ENST00000397852.5:c.2081-60G>C	ENSP00000380950.1:n.2081-60G>C
ENST00000397854.7:c.1910-60G>C	ENSP00000380952.3:n.1910-60G>C
ENST00000397857.5:c.2081-60G>C	ENSP00000380955.1:n.2081-60G>C
ENST00000475170.5:n.1481-60G>C
ENST00000479202.5:n.440-60G>C
ENST00000498666.5:n.4137-60G>C
ENST00000523323.5:c.*1908-60G>C	ENSP00000427732.1:n.*1908-60G>C
ENST00000610622.4:c.*772-60G>C	ENSP00000480700.1:n.*772-60G>C
NM_000211.4:c.2081-60G>C	NP_000202.3:n.2081-60G>C
NM_001127491.2:c.2081-60G>C	NP_001120963.2:n.2081-60G>C
NM_001303238.1:c.1874-60G>C	NP_001290167.1:n.1874-60G>C
XM_006724001.1:c.1874-60G>C	XP_006724064.1:n.1874-60G>C
XM_006724001.2:c.1874-60G>C	XP_006724064.1:n.1874-60G>C
NM_000211.5:c.2081-60G>C MANE Select	NP_000202.3:n.2081-60G>C
NM_001127491.3:c.2081-60G>C	NP_001120963.2:n.2081-60G>C
NM_001303238.2:c.1874-60G>C	NP_001290167.1:n.1874-60G>C