Canonical Allele Identifier: CA399805155
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44384946A>G , CM000679.2:g.44384946A>G GRCh38
NC_000017.10:g.42462314A>G , CM000679.1:g.42462314A>G GRCh37
NC_000017.9:g.39817840A>G NCBI36
NG_008331.1:g.9560T>C , LRG_479:g.9560T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.799+2T>C MANE Select ENSP00000262407.5:n.799+2T>C
ENST00000648408.1:c.230+2T>C
ENST00000262407.5:c.799+2T>C ENSP00000262407.5:n.799+2T>C
ENST00000589645.5:n.250+2T>C
ENST00000591990.5:n.161+2T>C
ENST00000592075.5:n.168+2T>C
ENST00000592226.5:n.39+218T>C
ENST00000592253.5:n.307+2T>C
ENST00000592944.1:n.481+2T>C
NM_000419.3:c.799+2T>C , LRG_479t1:c.799+2T>C NP_000410.2:n.799+2T>C
XM_011524749.1:c.799+2T>C XP_011523051.1:n.799+2T>C
XM_011524750.1:c.799+2T>C XP_011523052.1:n.799+2T>C
NM_000419.4:c.799+2T>C NP_000410.2:n.799+2T>C
NM_000419.5:c.799+2T>C MANE Select NP_000410.2:n.799+2T>C
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