Canonical Allele Identifier: CA2576290842

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44372519-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372519G>T , CM000679.2:g.44372519G>T	GRCh38
NC_000017.10:g.42449887G>T , CM000679.1:g.42449887G>T	GRCh37
NC_000017.9:g.39805413G>T	NCBI36
NG_008331.1:g.21987C>A , LRG_479:g.21987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3061-96C>A MANE Select	ENSP00000262407.5:n.3061-96C>A
ENST00000648408.1:c.2375-96C>A
ENST00000262407.5:c.3061-96C>A	ENSP00000262407.5:n.3061-96C>A
ENST00000587295.5:c.254-96C>A
ENST00000588098.1:c.38-96C>A
NM_000419.3:c.3061-96C>A , LRG_479t1:c.3061-96C>A	NP_000410.2:n.3061-96C>A
XM_011524749.1:c.2959-96C>A	XP_011523051.1:n.2959-96C>A
XM_011524750.1:c.2944-96C>A	XP_011523052.1:n.2944-96C>A
NM_000419.4:c.3061-96C>A	NP_000410.2:n.3061-96C>A
NM_000419.5:c.3061-96C>A MANE Select	NP_000410.2:n.3061-96C>A