Canonical Allele Identifier: CA410482371

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44886753-T-G
• MyVariant Identifiers: chr21:g.46306668T>G (hg19) ; chr21:g.44886753T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886753T>G , CM000683.2:g.44886753T>G	GRCh38
NC_000021.8:g.46306668T>G , CM000683.1:g.46306668T>G	GRCh37
NC_000021.7:g.45131096T>G	NCBI36
NG_007270.2:g.47086A>C , LRG_76:g.47086A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1437A>C
ENST00000302347.10:c.2302A>C	ENSP00000303242.6:p.Lys768Gln
ENST00000652462.1:c.2230A>C MANE Select	ENSP00000498780.1:p.Lys744Gln
ENST00000302347.9:c.2230A>C	ENSP00000303242.5:p.Lys744Gln
ENST00000355153.8:c.2230A>C	ENSP00000347279.4:p.Lys744Gln
ENST00000397850.6:c.2230A>C	ENSP00000380948.2:p.Lys744Gln
ENST00000397852.5:c.2230A>C	ENSP00000380950.1:p.Lys744Gln
ENST00000397854.7:c.2059A>C	ENSP00000380952.3:p.Lys687Gln
ENST00000397857.5:c.2230A>C	ENSP00000380955.1:p.Lys744Gln
ENST00000475170.5:n.1630A>C
ENST00000479202.5:n.589A>C
ENST00000498666.5:n.4286A>C
ENST00000523323.5:c.*2057A>C	ENSP00000427732.1:n.*2057A>C
ENST00000610622.4:c.*921A>C	ENSP00000480700.1:n.*921A>C
NM_000211.4:c.2230A>C	NP_000202.3:p.Lys744Gln
NM_001127491.2:c.2230A>C	NP_001120963.2:p.Lys744Gln
NM_001303238.1:c.2023A>C	NP_001290167.1:p.Lys675Gln
XM_006724001.1:c.2023A>C	XP_006724064.1:p.Lys675Gln
XM_006724001.2:c.2023A>C	XP_006724064.1:p.Lys675Gln
NM_000211.5:c.2230A>C MANE Select	NP_000202.3:p.Lys744Gln
NM_001127491.3:c.2230A>C	NP_001120963.2:p.Lys744Gln
NM_001303238.2:c.2023A>C	NP_001290167.1:p.Lys675Gln