Canonical Allele Identifier: CA2261364464
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372620_44372622delinsCCT , CM000679.2:g.44372620_44372622delinsCCT GRCh38
NC_000017.10:g.42449988_42449990delinsCCT , CM000679.1:g.42449988_42449990delinsCCT GRCh37
NC_000017.9:g.39805514_39805516delinsCCT NCBI36
NG_008331.1:g.21884_21886delinsAGG , LRG_479:g.21884_21886delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-199_3061-197delinsAGG MANE Select ENSP00000262407.5:n.3061-199_3061-197delinsAGG
ENST00000648408.1:c.2375-199_2375-197delinsAGG
ENST00000262407.5:c.3061-199_3061-197delinsAGG ENSP00000262407.5:n.3061-199_3061-197delinsAGG
ENST00000587295.5:c.254-199_254-197delinsAGG
ENST00000588098.1:c.38-199_38-197delinsAGG
NM_000419.3:c.3061-199_3061-197delinsAGG , LRG_479t1:c.3061-199_3061-197delinsAGG NP_000410.2:n.3061-199_3061-197delinsAGG
XM_011524749.1:c.2959-199_2959-197delinsAGG XP_011523051.1:n.2959-199_2959-197delinsAGG
XM_011524750.1:c.2944-199_2944-197delinsAGG XP_011523052.1:n.2944-199_2944-197delinsAGG
NM_000419.4:c.3061-199_3061-197delinsAGG NP_000410.2:n.3061-199_3061-197delinsAGG
NM_000419.5:c.3061-199_3061-197delinsAGG MANE Select NP_000410.2:n.3061-199_3061-197delinsAGG
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