Canonical Allele Identifier: CA410486206

Gene: ITGB2

Linked Data

• MyVariant Identifiers: chr21:g.46314891A>G (hg19) ; chr21:g.44894976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44894976A>G , CM000683.2:g.44894976A>G	GRCh38
NC_000021.8:g.46314891A>G , CM000683.1:g.46314891A>G	GRCh37
NC_000021.7:g.45139319A>G	NCBI36
NG_007270.2:g.38863T>C , LRG_76:g.38863T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1150T>C	ENSP00000303242.6:p.Tyr384His
ENST00000652462.1:c.1078T>C MANE Select	ENSP00000498780.1:p.Tyr360His
ENST00000302347.9:c.1078T>C	ENSP00000303242.5:p.Tyr360His
ENST00000355153.8:c.1078T>C	ENSP00000347279.4:p.Tyr360His
ENST00000397850.6:c.1078T>C	ENSP00000380948.2:p.Tyr360His
ENST00000397852.5:c.1078T>C	ENSP00000380950.1:p.Tyr360His
ENST00000397854.7:c.907T>C	ENSP00000380952.3:p.Tyr303His
ENST00000397857.5:c.1078T>C	ENSP00000380955.1:p.Tyr360His
ENST00000498666.5:n.1221T>C
ENST00000523323.5:c.*905T>C	ENSP00000427732.1:n.*905T>C
ENST00000610622.4:c.907T>C	ENSP00000480700.1:p.Tyr303His
NM_000211.4:c.1078T>C	NP_000202.3:p.Tyr360His
NM_001127491.2:c.1078T>C	NP_001120963.2:p.Tyr360His
NM_001303238.1:c.871T>C	NP_001290167.1:p.Tyr291His
XM_006724001.1:c.871T>C	XP_006724064.1:p.Tyr291His
XM_006724001.2:c.871T>C	XP_006724064.1:p.Tyr291His
NM_000211.5:c.1078T>C MANE Select	NP_000202.3:p.Tyr360His
NM_001127491.3:c.1078T>C	NP_001120963.2:p.Tyr360His
NM_001303238.2:c.871T>C	NP_001290167.1:p.Tyr291His