Canonical Allele Identifier: CA2261364473
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs2048507173
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372642T>G , CM000679.2:g.44372642T>G GRCh38
NC_000017.10:g.42450010T>G , CM000679.1:g.42450010T>G GRCh37
NC_000017.9:g.39805536T>G NCBI36
NG_008331.1:g.21864A>C , LRG_479:g.21864A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-219A>C MANE Select ENSP00000262407.5:n.3061-219A>C
ENST00000648408.1:c.2375-219A>C
ENST00000262407.5:c.3061-219A>C ENSP00000262407.5:n.3061-219A>C
ENST00000587295.5:c.254-219A>C
ENST00000588098.1:c.38-219A>C
NM_000419.3:c.3061-219A>C , LRG_479t1:c.3061-219A>C NP_000410.2:n.3061-219A>C
XM_011524749.1:c.2959-219A>C XP_011523051.1:n.2959-219A>C
XM_011524750.1:c.2944-219A>C XP_011523052.1:n.2944-219A>C
NM_000419.4:c.3061-219A>C NP_000410.2:n.3061-219A>C
NM_000419.5:c.3061-219A>C MANE Select NP_000410.2:n.3061-219A>C
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