Canonical Allele Identifier: CA2261367723
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379565T= , CM000679.2:g.44379565T= GRCh38
NC_000017.10:g.42456933T= , CM000679.1:g.42456933T= GRCh37
NC_000017.9:g.39812459T= NCBI36
NG_008331.1:g.14941A= , LRG_479:g.14941A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+124A= MANE Select ENSP00000262407.5:n.1878+124A=
ENST00000648408.1:c.1309+124A=
ENST00000262407.5:c.1878+124A= ENSP00000262407.5:n.1878+124A=
ENST00000592462.5:n.673+124A=
NM_000419.3:c.1878+124A= , LRG_479t1:c.1878+124A= NP_000410.2:n.1878+124A=
XM_011524749.1:c.1878+124A= XP_011523051.1:n.1878+124A=
XM_011524750.1:c.1878+124A= XP_011523052.1:n.1878+124A=
NM_000419.4:c.1878+124A= NP_000410.2:n.1878+124A=
NM_000419.5:c.1878+124A= MANE Select NP_000410.2:n.1878+124A=