Canonical Allele Identifier: CA2261365165
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374282T= , CM000679.2:g.44374282T= GRCh38
NC_000017.10:g.42451650T= , CM000679.1:g.42451650T= GRCh37
NC_000017.9:g.39807176T= NCBI36
NG_008331.1:g.20224A= , LRG_479:g.20224A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3060+72A= MANE Select ENSP00000262407.5:n.3060+72A=
ENST00000648408.1:c.2374+377A=
ENST00000262407.5:c.3060+72A= ENSP00000262407.5:n.3060+72A=
ENST00000587295.5:c.253+1551A=
ENST00000588098.1:c.37+377A=
ENST00000592462.5:n.2831A=
NM_000419.3:c.3060+72A= , LRG_479t1:c.3060+72A= NP_000410.2:n.3060+72A=
XM_011524749.1:c.2958+72A= XP_011523051.1:n.2958+72A=
XM_011524750.1:c.2943+377A= XP_011523052.1:n.2943+377A=
NM_000419.4:c.3060+72A= NP_000410.2:n.3060+72A=
NM_000419.5:c.3060+72A= MANE Select NP_000410.2:n.3060+72A=