Canonical Allele Identifier: CA2261364441
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372555_44372556delinsAT , CM000679.2:g.44372555_44372556delinsAT GRCh38
NC_000017.10:g.42449923_42449924delinsAT , CM000679.1:g.42449923_42449924delinsAT GRCh37
NC_000017.9:g.39805449_39805450delinsAT NCBI36
NG_008331.1:g.21950_21951delinsAT , LRG_479:g.21950_21951delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-133_3061-132delinsAT MANE Select ENSP00000262407.5:n.3061-133_3061-132delinsAT
ENST00000648408.1:c.2375-133_2375-132delinsAT
ENST00000262407.5:c.3061-133_3061-132delinsAT ENSP00000262407.5:n.3061-133_3061-132delinsAT
ENST00000587295.5:c.254-133_254-132delinsAT
ENST00000588098.1:c.38-133_38-132delinsAT
NM_000419.3:c.3061-133_3061-132delinsAT , LRG_479t1:c.3061-133_3061-132delinsAT NP_000410.2:n.3061-133_3061-132delinsAT
XM_011524749.1:c.2959-133_2959-132delinsAT XP_011523051.1:n.2959-133_2959-132delinsAT
XM_011524750.1:c.2944-133_2944-132delinsAT XP_011523052.1:n.2944-133_2944-132delinsAT
NM_000419.4:c.3061-133_3061-132delinsAT NP_000410.2:n.3061-133_3061-132delinsAT
NM_000419.5:c.3061-133_3061-132delinsAT MANE Select NP_000410.2:n.3061-133_3061-132delinsAT
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