Canonical Allele Identifier: CA10062534

Gene: ITGB2

Linked Data

• ClinVar Variation Id: 1440950
• ClinVar RCV Id: RCV001978983
• dbSNP Id: rs750002294
• ExAC: 21:46306726 C / T
• gnomAD v2: 21-46306726-C-T
• gnomAD v3: 21-44886811-C-T
• gnomAD v4: 21-44886811-C-T
• MyVariant Identifiers: chr21:g.46306726C>T (hg19) ; chr21:g.44886811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886811C>T , CM000683.2:g.44886811C>T	GRCh38
NC_000021.8:g.46306726C>T , CM000683.1:g.46306726C>T	GRCh37
NC_000021.7:g.45131154C>T	NCBI36
NG_007270.2:g.47028G>A , LRG_76:g.47028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1379G>A
ENST00000302347.10:c.2244G>A	ENSP00000303242.6:p.Lys748=
ENST00000652462.1:c.2172G>A MANE Select	ENSP00000498780.1:p.Lys724=
ENST00000302347.9:c.2172G>A	ENSP00000303242.5:p.Lys724=
ENST00000355153.8:c.2172G>A	ENSP00000347279.4:p.Lys724=
ENST00000397850.6:c.2172G>A	ENSP00000380948.2:p.Lys724=
ENST00000397852.5:c.2172G>A	ENSP00000380950.1:p.Lys724=
ENST00000397854.7:c.2001G>A	ENSP00000380952.3:p.Lys667=
ENST00000397857.5:c.2172G>A	ENSP00000380955.1:p.Lys724=
ENST00000475170.5:n.1572G>A
ENST00000479202.5:n.531G>A
ENST00000498666.5:n.4228G>A
ENST00000523323.5:c.*1999G>A	ENSP00000427732.1:n.*1999G>A
ENST00000610622.4:c.*863G>A	ENSP00000480700.1:n.*863G>A
NM_000211.4:c.2172G>A	NP_000202.3:p.Lys724=
NM_001127491.2:c.2172G>A	NP_001120963.2:p.Lys724=
NM_001303238.1:c.1965G>A	NP_001290167.1:p.Lys655=
XM_006724001.1:c.1965G>A	XP_006724064.1:p.Lys655=
XM_006724001.2:c.1965G>A	XP_006724064.1:p.Lys655=
NM_000211.5:c.2172G>A MANE Select	NP_000202.3:p.Lys724=
NM_001127491.3:c.2172G>A	NP_001120963.2:p.Lys724=
NM_001303238.2:c.1965G>A	NP_001290167.1:p.Lys655=