Canonical Allele Identifier: CA512549518

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44889281-C-T
• MyVariant Identifiers: chr21:g.46309196C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44889281C>T , CM000683.2:g.44889281C>T	GRCh38
NC_000021.8:g.46309196C>T , CM000683.1:g.46309196C>T	GRCh37
NC_000021.7:g.45133624C>T	NCBI36
NG_007270.2:g.44558G>A , LRG_76:g.44558G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696946.1:n.1079G>A
ENST00000302347.10:c.1944G>A	ENSP00000303242.6:p.Lys648=
ENST00000652462.1:c.1872G>A MANE Select	ENSP00000498780.1:p.Lys624=
ENST00000302347.9:c.1872G>A	ENSP00000303242.5:p.Lys624=
ENST00000355153.8:c.1872G>A	ENSP00000347279.4:p.Lys624=
ENST00000397850.6:c.1872G>A	ENSP00000380948.2:p.Lys624=
ENST00000397852.5:c.1872G>A	ENSP00000380950.1:p.Lys624=
ENST00000397854.7:c.1701G>A	ENSP00000380952.3:p.Lys567=
ENST00000397857.5:c.1872G>A	ENSP00000380955.1:p.Lys624=
ENST00000475170.5:n.1272G>A
ENST00000498666.5:n.3928G>A
ENST00000523323.5:c.*1699G>A	ENSP00000427732.1:n.*1699G>A
ENST00000610622.4:c.*563G>A	ENSP00000480700.1:n.*563G>A
NM_000211.4:c.1872G>A	NP_000202.3:p.Lys624=
NM_001127491.2:c.1872G>A	NP_001120963.2:p.Lys624=
NM_001303238.1:c.1665G>A	NP_001290167.1:p.Lys555=
XM_006724001.1:c.1665G>A	XP_006724064.1:p.Lys555=
XM_006724001.2:c.1665G>A	XP_006724064.1:p.Lys555=
NM_000211.5:c.1872G>A MANE Select	NP_000202.3:p.Lys624=
NM_001127491.3:c.1872G>A	NP_001120963.2:p.Lys624=
NM_001303238.2:c.1665G>A	NP_001290167.1:p.Lys555=