Canonical Allele Identifier: CA2576291342
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v3: 17-44384218-T-G
gnomAD v4: 17-44384218-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44384218T>G , CM000679.2:g.44384218T>G GRCh38
NC_000017.10:g.42461586T>G , CM000679.1:g.42461586T>G GRCh37
NC_000017.9:g.39817112T>G NCBI36
NG_008331.1:g.10288A>C , LRG_479:g.10288A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.892-80A>C MANE Select ENSP00000262407.5:n.892-80A>C
ENST00000648408.1:c.323-80A>C
ENST00000262407.5:c.892-80A>C ENSP00000262407.5:n.892-80A>C
ENST00000589645.5:n.343-80A>C
ENST00000591990.5:n.437-80A>C
ENST00000592075.5:n.261-80A>C
ENST00000592226.5:n.132-80A>C
ENST00000592253.5:n.400-80A>C
NM_000419.3:c.892-80A>C , LRG_479t1:c.892-80A>C NP_000410.2:n.892-80A>C
XM_011524749.1:c.892-80A>C XP_011523051.1:n.892-80A>C
XM_011524750.1:c.892-80A>C XP_011523052.1:n.892-80A>C
NM_000419.4:c.892-80A>C NP_000410.2:n.892-80A>C
NM_000419.5:c.892-80A>C MANE Select NP_000410.2:n.892-80A>C
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