Canonical Allele Identifier: CA2963260859
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379791_44379792insCTCAA , CM000679.2:g.44379791_44379792insCTCAA GRCh38
NC_000017.10:g.42457159_42457160insCTCAA , CM000679.1:g.42457159_42457160insCTCAA GRCh37
NC_000017.9:g.39812685_39812686insCTCAA NCBI36
NG_008331.1:g.14714_14715insTTGAG , LRG_479:g.14714_14715insTTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.1775_1776insTTGAG MANE Select ENSP00000262407.5:p.Lys592AsnfsTer2
ENST00000648408.1:c.1206_1207insTTGAG
ENST00000262407.5:c.1775_1776insTTGAG ENSP00000262407.5:p.Lys592AsnfsTer2
ENST00000592462.5:n.570_571insTTGAG
NM_000419.3:c.1775_1776insTTGAG , LRG_479t1:c.1775_1776insTTGAG NP_000410.2:p.Lys592AsnfsTer2
XM_011524749.1:c.1775_1776insTTGAG XP_011523051.1:p.Lys592AsnfsTer2
XM_011524750.1:c.1775_1776insTTGAG XP_011523052.1:p.Lys592AsnfsTer2
NM_000419.4:c.1775_1776insTTGAG NP_000410.2:p.Lys592AsnfsTer2
NM_000419.5:c.1775_1776insTTGAG MANE Select NP_000410.2:p.Lys592AsnfsTer2
Search 100 bp 5'
Search 100 bp 3'