Canonical Allele Identifier: CA2638217469
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44379710-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379712del , CM000679.2:g.44379712del GRCh38
NC_000017.10:g.42457080del , CM000679.1:g.42457080del GRCh37
NC_000017.9:g.39812606del NCBI36
NG_008331.1:g.14795del , LRG_479:g.14795del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1856del MANE Select ENSP00000262407.5:p.Gly619GlufsTer?
ENST00000648408.1:c.1287del
ENST00000262407.5:c.1856del ENSP00000262407.5:p.Gly619GlufsTer?
ENST00000592462.5:n.651del
NM_000419.3:c.1856del , LRG_479t1:c.1856del NP_000410.2:p.Gly619GlufsTer?
XM_011524749.1:c.1856del XP_011523051.1:p.Gly619GlufsTer?
XM_011524750.1:c.1856del XP_011523052.1:p.Gly619GlufsTer?
NM_000419.4:c.1856del NP_000410.2:p.Gly619GlufsTer?
NM_000419.5:c.1856del MANE Select NP_000410.2:p.Gly619GlufsTer?
Search 100 bp 5'
Search 100 bp 3'