Canonical Allele Identifier: CA2261364316
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372312C= , CM000679.2:g.44372312C= GRCh38
NC_000017.10:g.42449680C= , CM000679.1:g.42449680C= GRCh37
NC_000017.9:g.39805206C= NCBI36
NG_008331.1:g.22194G= , LRG_479:g.22194G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.*52G= MANE Select ENSP00000262407.5:n.*52G=
ENST00000648408.1:c.2486G=
ENST00000262407.5:c.*52G= ENSP00000262407.5:n.*52G=
ENST00000587295.5:c.365G=
ENST00000588098.1:c.149G=
NM_000419.3:c.*52G= , LRG_479t1:c.*52G= NP_000410.2:n.*52G=
XM_011524749.1:c.*52G= XP_011523051.1:n.*52G=
XM_011524750.1:c.*52G= XP_011523052.1:n.*52G=
NM_000419.4:c.*52G= NP_000410.2:n.*52G=
NM_000419.5:c.*52G= MANE Select NP_000410.2:n.*52G=