Canonical Allele Identifier: CA2261364367
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372407_44372408delinsCG , CM000679.2:g.44372407_44372408delinsCG GRCh38
NC_000017.10:g.42449775_42449776delinsCG , CM000679.1:g.42449775_42449776delinsCG GRCh37
NC_000017.9:g.39805301_39805302delinsCG NCBI36
NG_008331.1:g.22098_22099delinsCG , LRG_479:g.22098_22099delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3076_3077delinsCG MANE Select ENSP00000262407.5:p.Arg1026=
ENST00000648408.1:c.2390_2391delinsCG
ENST00000262407.5:c.3076_3077delinsCG ENSP00000262407.5:p.Arg1026=
ENST00000587295.5:c.269_270delinsCG
ENST00000588098.1:c.53_54delinsCG
NM_000419.3:c.3076_3077delinsCG , LRG_479t1:c.3076_3077delinsCG NP_000410.2:p.Arg1026=
XM_011524749.1:c.2974_2975delinsCG XP_011523051.1:p.Arg992=
XM_011524750.1:c.2959_2960delinsCG XP_011523052.1:p.Arg987=
NM_000419.4:c.3076_3077delinsCG NP_000410.2:p.Arg1026=
NM_000419.5:c.3076_3077delinsCG MANE Select NP_000410.2:p.Arg1026=
Search 100 bp 5'
Search 100 bp 3'