Canonical Allele Identifier: CA2261364326
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372327G= , CM000679.2:g.44372327G= GRCh38
NC_000017.10:g.42449695G= , CM000679.1:g.42449695G= GRCh37
NC_000017.9:g.39805221G= NCBI36
NG_008331.1:g.22179C= , LRG_479:g.22179C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.*37C= MANE Select ENSP00000262407.5:n.*37C=
ENST00000648408.1:c.2471C=
ENST00000262407.5:c.*37C= ENSP00000262407.5:n.*37C=
ENST00000587295.5:c.350C=
ENST00000588098.1:c.134C=
NM_000419.3:c.*37C= , LRG_479t1:c.*37C= NP_000410.2:n.*37C=
XM_011524749.1:c.*37C= XP_011523051.1:n.*37C=
XM_011524750.1:c.*37C= XP_011523052.1:n.*37C=
NM_000419.4:c.*37C= NP_000410.2:n.*37C=
NM_000419.5:c.*37C= MANE Select NP_000410.2:n.*37C=