Canonical Allele Identifier: CA410476076

Gene: ITGB2

Linked Data

• MyVariant Identifiers: chr21:g.46321466C>A (hg19) ; chr21:g.44901551C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44901551C>A , CM000683.2:g.44901551C>A	GRCh38
NC_000021.8:g.46321466C>A , CM000683.1:g.46321466C>A	GRCh37
NC_000021.7:g.45145894C>A	NCBI36
NG_007270.2:g.32288G>T , LRG_76:g.32288G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302347.10:c.682G>T	ENSP00000303242.6:p.Gly228Ter
ENST00000652462.1:c.682G>T MANE Select	ENSP00000498780.1:p.Gly228Ter
ENST00000302347.9:c.682G>T	ENSP00000303242.5:p.Gly228Ter
ENST00000320216.10:c.655G>T	ENSP00000317697.6:p.Gly219Ter
ENST00000355153.8:c.682G>T	ENSP00000347279.4:p.Gly228Ter
ENST00000397850.6:c.682G>T	ENSP00000380948.2:p.Gly228Ter
ENST00000397852.5:c.682G>T	ENSP00000380950.1:p.Gly228Ter
ENST00000397854.7:c.511G>T	ENSP00000380952.3:p.Gly171Ter
ENST00000397857.5:c.682G>T	ENSP00000380955.1:p.Gly228Ter
ENST00000498666.5:n.825G>T
ENST00000521987.1:n.563G>T
ENST00000523323.5:c.*509G>T	ENSP00000427732.1:n.*509G>T
ENST00000610622.4:c.511G>T	ENSP00000480700.1:p.Gly171Ter
NM_000211.4:c.682G>T	NP_000202.3:p.Gly228Ter
NM_001127491.2:c.682G>T	NP_001120963.2:p.Gly228Ter
NM_001303238.1:c.475G>T	NP_001290167.1:p.Gly159Ter
XM_006724001.1:c.475G>T	XP_006724064.1:p.Gly159Ter
XM_006724001.2:c.475G>T	XP_006724064.1:p.Gly159Ter
NM_000211.5:c.682G>T MANE Select	NP_000202.3:p.Gly228Ter
NM_001127491.3:c.682G>T	NP_001120963.2:p.Gly228Ter
NM_001303238.2:c.475G>T	NP_001290167.1:p.Gly159Ter