Canonical Allele Identifier: CA2261365366
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374691G= , CM000679.2:g.44374691G= GRCh38
NC_000017.10:g.42452059G= , CM000679.1:g.42452059G= GRCh37
NC_000017.9:g.39807585G= NCBI36
NG_008331.1:g.19815C= , LRG_479:g.19815C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2911C= MANE Select ENSP00000262407.5:p.Pro971=
ENST00000648408.1:c.2342C=
ENST00000262407.5:c.2911C= ENSP00000262407.5:p.Pro971=
ENST00000587295.5:c.253+1142C=
ENST00000588098.1:c.5C=
ENST00000592462.5:n.2422C=
NM_000419.3:c.2911C= , LRG_479t1:c.2911C= NP_000410.2:p.Pro971=
XM_011524749.1:c.2842-221C= XP_011523051.1:n.2842-221C=
XM_011524750.1:c.2911C= XP_011523052.1:p.Pro971=
NM_000419.4:c.2911C= NP_000410.2:p.Pro971=
NM_000419.5:c.2911C= MANE Select NP_000410.2:p.Pro971=