Canonical Allele Identifier: CA2261367760
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379678C= , CM000679.2:g.44379678C= GRCh38
NC_000017.10:g.42457046C= , CM000679.1:g.42457046C= GRCh37
NC_000017.9:g.39812572C= NCBI36
NG_008331.1:g.14828G= , LRG_479:g.14828G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+11G= MANE Select ENSP00000262407.5:n.1878+11G=
ENST00000648408.1:c.1309+11G=
ENST00000262407.5:c.1878+11G= ENSP00000262407.5:n.1878+11G=
ENST00000592462.5:n.673+11G=
NM_000419.3:c.1878+11G= , LRG_479t1:c.1878+11G= NP_000410.2:n.1878+11G=
XM_011524749.1:c.1878+11G= XP_011523051.1:n.1878+11G=
XM_011524750.1:c.1878+11G= XP_011523052.1:n.1878+11G=
NM_000419.4:c.1878+11G= NP_000410.2:n.1878+11G=
NM_000419.5:c.1878+11G= MANE Select NP_000410.2:n.1878+11G=