Canonical Allele Identifier: CA2837995121
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372391_44372392insCA , CM000679.2:g.44372391_44372392insCA GRCh38
NC_000017.10:g.42449759_42449760insCA , CM000679.1:g.42449759_42449760insCA GRCh37
NC_000017.9:g.39805285_39805286insCA NCBI36
NG_008331.1:g.22114_22115insTG , LRG_479:g.22114_22115insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3092_3093insTG MANE Select ENSP00000262407.5:p.Glu1032GlyfsTer?
ENST00000648408.1:c.2406_2407insTG
ENST00000262407.5:c.3092_3093insTG ENSP00000262407.5:p.Glu1032GlyfsTer?
ENST00000587295.5:c.285_286insTG
ENST00000588098.1:c.69_70insTG
NM_000419.3:c.3092_3093insTG , LRG_479t1:c.3092_3093insTG NP_000410.2:p.Glu1032GlyfsTer?
XM_011524749.1:c.2990_2991insTG XP_011523051.1:p.Glu998GlyfsTer?
XM_011524750.1:c.2975_2976insTG XP_011523052.1:p.Glu993GlyfsTer?
NM_000419.4:c.3092_3093insTG NP_000410.2:p.Glu1032GlyfsTer?
NM_000419.5:c.3092_3093insTG MANE Select NP_000410.2:p.Glu1032GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'