Canonical Allele Identifier: CA10653665

Gene: ITGB2

Linked Data

• ClinVar Variation Id: 340134
• ClinVar RCV Id: RCV000322595 ; RCV001618603
• dbSNP Id: rs684
• gnomAD v2: 21-46306161-C-T
• gnomAD v3: 21-44886246-C-T
• gnomAD v4: 21-44886246-C-T
• MyVariant Identifiers: chr21:g.46306161C>T (hg19) ; chr21:g.44886246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886246C>T , CM000683.2:g.44886246C>T	GRCh38
NC_000021.8:g.46306161C>T , CM000683.1:g.46306161C>T	GRCh37
NC_000021.7:g.45130589C>T	NCBI36
NG_007270.2:g.47593G>A , LRG_76:g.47593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1639G>A
ENST00000302347.10:c.*122G>A	ENSP00000303242.6:n.*122G>A
ENST00000652462.1:c.*122G>A MANE Select	ENSP00000498780.1:n.*122G>A
ENST00000302347.9:c.*122G>A	ENSP00000303242.5:n.*122G>A
ENST00000355153.8:c.*122G>A	ENSP00000347279.4:n.*122G>A
ENST00000397850.6:c.*122G>A	ENSP00000380948.2:n.*122G>A
ENST00000397852.5:c.*122G>A	ENSP00000380950.1:n.*122G>A
ENST00000397854.7:c.*122G>A	ENSP00000380952.3:n.*122G>A
ENST00000397857.5:c.*122G>A	ENSP00000380955.1:n.*122G>A
ENST00000475170.5:n.1832G>A
ENST00000498666.5:n.4488G>A
ENST00000523323.5:c.*2259G>A	ENSP00000427732.1:n.*2259G>A
NM_000211.4:c.*122G>A	NP_000202.3:n.*122G>A
NM_001127491.2:c.*122G>A	NP_001120963.2:n.*122G>A
NM_001303238.1:c.*122G>A	NP_001290167.1:n.*122G>A
XM_006724001.1:c.*122G>A	XP_006724064.1:n.*122G>A
XM_006724001.2:c.*122G>A	XP_006724064.1:n.*122G>A
NM_000211.5:c.*122G>A MANE Select	NP_000202.3:n.*122G>A
NM_001127491.3:c.*122G>A	NP_001120963.2:n.*122G>A
NM_001303238.2:c.*122G>A	NP_001290167.1:n.*122G>A