Canonical Allele Identifier: CA2261364392
Gene: ITGA2B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372450G= , CM000679.2:g.44372450G= GRCh38
NC_000017.10:g.42449818G= , CM000679.1:g.42449818G= GRCh37
NC_000017.9:g.39805344G= NCBI36
NG_008331.1:g.22056C= , LRG_479:g.22056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-27C= MANE Select ENSP00000262407.5:n.3061-27C=
ENST00000648408.1:c.2375-27C=
ENST00000262407.5:c.3061-27C= ENSP00000262407.5:n.3061-27C=
ENST00000587295.5:c.254-27C=
ENST00000588098.1:c.38-27C=
NM_000419.3:c.3061-27C= , LRG_479t1:c.3061-27C= NP_000410.2:n.3061-27C=
XM_011524749.1:c.2959-27C= XP_011523051.1:n.2959-27C=
XM_011524750.1:c.2944-27C= XP_011523052.1:n.2944-27C=
NM_000419.4:c.3061-27C= NP_000410.2:n.3061-27C=
NM_000419.5:c.3061-27C= MANE Select NP_000410.2:n.3061-27C=
Search 100 bp 5'
Search 100 bp 3'