Canonical Allele Identifier: CA2963260866
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379792_44379793insCAATG , CM000679.2:g.44379792_44379793insCAATG GRCh38
NC_000017.10:g.42457160_42457161insCAATG , CM000679.1:g.42457160_42457161insCAATG GRCh37
NC_000017.9:g.39812686_39812687insCAATG NCBI36
NG_008331.1:g.14713_14714insCATTG , LRG_479:g.14713_14714insCATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.1774_1775insCATTG MANE Select ENSP00000262407.5:p.Lys592ThrfsTer4
ENST00000648408.1:c.1205_1206insCATTG
ENST00000262407.5:c.1774_1775insCATTG ENSP00000262407.5:p.Lys592ThrfsTer4
ENST00000592462.5:n.569_570insCATTG
NM_000419.3:c.1774_1775insCATTG , LRG_479t1:c.1774_1775insCATTG NP_000410.2:p.Lys592ThrfsTer4
XM_011524749.1:c.1774_1775insCATTG XP_011523051.1:p.Lys592ThrfsTer4
XM_011524750.1:c.1774_1775insCATTG XP_011523052.1:p.Lys592ThrfsTer4
NM_000419.4:c.1774_1775insCATTG NP_000410.2:p.Lys592ThrfsTer4
NM_000419.5:c.1774_1775insCATTG MANE Select NP_000410.2:p.Lys592ThrfsTer4
Search 100 bp 5'
Search 100 bp 3'