Canonical Allele Identifier: CA410485879

Gene: ITGB2

Linked Data

• MyVariant Identifiers: chr21:g.46313390A>T (hg19) ; chr21:g.44893475A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893475A>T , CM000683.2:g.44893475A>T	GRCh38
NC_000021.8:g.46313390A>T , CM000683.1:g.46313390A>T	GRCh37
NC_000021.7:g.45137818A>T	NCBI36
NG_007270.2:g.40364T>A , LRG_76:g.40364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1225T>A	ENSP00000303242.6:p.Phe409Ile
ENST00000652462.1:c.1153T>A MANE Select	ENSP00000498780.1:p.Phe385Ile
ENST00000302347.9:c.1153T>A	ENSP00000303242.5:p.Phe385Ile
ENST00000355153.8:c.1153T>A	ENSP00000347279.4:p.Phe385Ile
ENST00000397850.6:c.1153T>A	ENSP00000380948.2:p.Phe385Ile
ENST00000397852.5:c.1153T>A	ENSP00000380950.1:p.Phe385Ile
ENST00000397854.7:c.982T>A	ENSP00000380952.3:p.Phe328Ile
ENST00000397857.5:c.1153T>A	ENSP00000380955.1:p.Phe385Ile
ENST00000475170.5:n.553T>A
ENST00000498666.5:n.2722T>A
ENST00000523323.5:c.*980T>A	ENSP00000427732.1:n.*980T>A
ENST00000610622.4:c.982T>A	ENSP00000480700.1:p.Phe328Ile
NM_000211.4:c.1153T>A	NP_000202.3:p.Phe385Ile
NM_001127491.2:c.1153T>A	NP_001120963.2:p.Phe385Ile
NM_001303238.1:c.946T>A	NP_001290167.1:p.Phe316Ile
XM_006724001.1:c.946T>A	XP_006724064.1:p.Phe316Ile
XM_006724001.2:c.946T>A	XP_006724064.1:p.Phe316Ile
NM_000211.5:c.1153T>A MANE Select	NP_000202.3:p.Phe385Ile
NM_001127491.3:c.1153T>A	NP_001120963.2:p.Phe385Ile
NM_001303238.2:c.946T>A	NP_001290167.1:p.Phe316Ile