Canonical Allele Identifier: CA410481692

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44910725C>G , CM000683.2:g.44910725C>G	GRCh38
NC_000021.8:g.46330640C>G , CM000683.1:g.46330640C>G	GRCh37
NC_000021.7:g.45155068C>G	NCBI36
NG_007270.2:g.23114G>C , LRG_76:g.23114G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000211.5:c.58G>C MANE Select	NP_000202.3:p.Val20Leu
ENST00000652462.1:c.58G>C MANE Select	ENSP00000498780.1:p.Val20Leu
NM_000211.4:c.58G>C	NP_000202.3:p.Val20Leu
NM_001127491.2:c.58G>C	NP_001120963.2:p.Val20Leu
NM_001127491.3:c.58G>C	NP_001120963.2:p.Val20Leu
NM_001303238.1:c.-193G>C	NP_001290167.1:n.-193G>C
NM_001303238.2:c.-193G>C	NP_001290167.1:n.-193G>C
ENST00000302347.10:c.58G>C	ENSP00000303242.6:p.Val20Leu
ENST00000302347.9:c.58G>C	ENSP00000303242.5:p.Val20Leu
ENST00000355153.8:c.58G>C	ENSP00000347279.4:p.Val20Leu
ENST00000397846.7:c.58G>C	ENSP00000380944.3:p.Val20Leu
ENST00000397850.6:c.58G>C	ENSP00000380948.2:p.Val20Leu
ENST00000397852.5:c.58G>C	ENSP00000380950.1:p.Val20Leu
ENST00000397854.7:c.58G>C	ENSP00000380952.3:p.Val20Leu
ENST00000397857.5:c.58G>C	ENSP00000380955.1:p.Val20Leu
ENST00000479849.1:n.17G>C
ENST00000498666.5:n.201G>C
ENST00000517563.5:c.58G>C	ENSP00000428413.1:p.Val20Leu
ENST00000517819.5:c.58G>C	ENSP00000428870.1:p.Val20Leu
ENST00000518033.1:n.168G>C
ENST00000520389.5:c.58G>C	ENSP00000428434.1:p.Val20Leu
ENST00000521987.1:n.113-7190G>C
ENST00000521995.1:c.58G>C	ENSP00000429683.1:p.Val20Leu
ENST00000522688.5:c.-275G>C	ENSP00000428125.1:n.-275G>C
ENST00000522931.5:c.58G>C	ENSP00000428979.1:p.Val20Leu
ENST00000523323.5:c.58G>C	ENSP00000427732.1:p.Gly20Arg
ENST00000523663.5:c.58G>C	ENSP00000428503.1:p.Val20Leu
ENST00000524251.1:c.-318G>C	ENSP00000430901.1:n.-318G>C
ENST00000610622.4:c.58G>C	ENSP00000480700.1:p.Val20Leu
XM_006724001.1:c.-275G>C	XP_006724064.1:n.-275G>C
XM_006724001.2:c.-275G>C	XP_006724064.1:n.-275G>C