Canonical Allele Identifier: CA249765

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44910759C>A , CM000683.2:g.44910759C>A	GRCh38
NC_000021.8:g.46330674C>A , CM000683.1:g.46330674C>A	GRCh37
NC_000021.7:g.45155102C>A	NCBI36
NG_007270.2:g.23080G>T , LRG_76:g.23080G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.24G>T	ENSP00000303242.6:p.Leu8=
ENST00000652462.1:c.24G>T MANE Select	ENSP00000498780.1:p.Leu8=
ENST00000302347.9:c.24G>T	ENSP00000303242.5:p.Leu8=
ENST00000355153.8:c.24G>T	ENSP00000347279.4:p.Leu8=
ENST00000397846.7:c.24G>T	ENSP00000380944.3:p.Leu8=
ENST00000397850.6:c.24G>T	ENSP00000380948.2:p.Leu8=
ENST00000397852.5:c.24G>T	ENSP00000380950.1:p.Leu8=
ENST00000397854.7:c.24G>T	ENSP00000380952.3:p.Leu8=
ENST00000397857.5:c.24G>T	ENSP00000380955.1:p.Leu8=
ENST00000498666.5:n.167G>T
ENST00000517563.5:c.24G>T	ENSP00000428413.1:p.Leu8=
ENST00000517819.5:c.24G>T	ENSP00000428870.1:p.Leu8=
ENST00000518033.1:n.134G>T
ENST00000520389.5:c.24G>T	ENSP00000428434.1:p.Leu8=
ENST00000521987.1:n.113-7224G>T
ENST00000521995.1:c.24G>T	ENSP00000429683.1:p.Leu8=
ENST00000522688.5:c.-309G>T	ENSP00000428125.1:n.-309G>T
ENST00000522931.5:c.24G>T	ENSP00000428979.1:p.Leu8=
ENST00000523323.5:c.24G>T	ENSP00000427732.1:p.Leu8=
ENST00000523663.5:c.24G>T	ENSP00000428503.1:p.Leu8=
ENST00000524251.1:c.-352G>T	ENSP00000430901.1:n.-352G>T
ENST00000610622.4:c.24G>T	ENSP00000480700.1:p.Leu8=
NM_000211.4:c.24G>T	NP_000202.3:p.Leu8=
NM_001127491.2:c.24G>T	NP_001120963.2:p.Leu8=
NM_001303238.1:c.-227G>T	NP_001290167.1:n.-227G>T
XM_006724001.1:c.-309G>T	XP_006724064.1:n.-309G>T
XM_006724001.2:c.-309G>T	XP_006724064.1:n.-309G>T
NM_000211.5:c.24G>T MANE Select	NP_000202.3:p.Leu8=
NM_001127491.3:c.24G>T	NP_001120963.2:p.Leu8=
NM_001303238.2:c.-227G>T	NP_001290167.1:n.-227G>T