Canonical Allele Identifier: CA2638217073

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44384505-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384505C>T , CM000679.2:g.44384505C>T	GRCh38
NC_000017.10:g.42461873C>T , CM000679.1:g.42461873C>T	GRCh37
NC_000017.9:g.39817399C>T	NCBI36
NG_008331.1:g.10001G>A , LRG_479:g.10001G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.847+33G>A MANE Select	ENSP00000262407.5:n.847+33G>A
ENST00000648408.1:c.278+33G>A
ENST00000262407.5:c.847+33G>A	ENSP00000262407.5:n.847+33G>A
ENST00000589645.5:n.298+33G>A
ENST00000591990.5:n.242G>A
ENST00000592075.5:n.216+33G>A
ENST00000592226.5:n.87+33G>A
ENST00000592253.5:n.355+33G>A
ENST00000592944.1:n.529+33G>A
NM_000419.3:c.847+33G>A , LRG_479t1:c.847+33G>A	NP_000410.2:n.847+33G>A
XM_011524749.1:c.847+33G>A	XP_011523051.1:n.847+33G>A
XM_011524750.1:c.847+33G>A	XP_011523052.1:n.847+33G>A
NM_000419.4:c.847+33G>A	NP_000410.2:n.847+33G>A
NM_000419.5:c.847+33G>A MANE Select	NP_000410.2:n.847+33G>A