Canonical Allele Identifier: CA399805152

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384587T>C , CM000679.2:g.44384587T>C	GRCh38
NC_000017.10:g.42461955T>C , CM000679.1:g.42461955T>C	GRCh37
NC_000017.9:g.39817481T>C	NCBI36
NG_008331.1:g.9919A>G , LRG_479:g.9919A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.800-2A>G MANE Select	NP_000410.2:n.800-2A>G
ENST00000262407.6:c.800-2A>G MANE Select	ENSP00000262407.5:n.800-2A>G
NM_000419.3:c.800-2A>G , LRG_479t1:c.800-2A>G	NP_000410.2:n.800-2A>G
NM_000419.4:c.800-2A>G	NP_000410.2:n.800-2A>G
ENST00000262407.5:c.800-2A>G	ENSP00000262407.5:n.800-2A>G
ENST00000589645.5:n.251-2A>G
ENST00000591990.5:n.162-2A>G
ENST00000592075.5:n.169-2A>G
ENST00000592226.5:n.40-2A>G
ENST00000592253.5:n.308-2A>G
ENST00000592944.1:n.482-2A>G
ENST00000648408.1:c.231-2A>G
XM_011524749.1:c.800-2A>G	XP_011523051.1:n.800-2A>G
XM_011524750.1:c.800-2A>G	XP_011523052.1:n.800-2A>G