Canonical Allele Identifier: CA2261364475
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs2048507197
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372643T>C , CM000679.2:g.44372643T>C GRCh38
NC_000017.10:g.42450011T>C , CM000679.1:g.42450011T>C GRCh37
NC_000017.9:g.39805537T>C NCBI36
NG_008331.1:g.21863A>G , LRG_479:g.21863A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-220A>G MANE Select ENSP00000262407.5:n.3061-220A>G
ENST00000648408.1:c.2375-220A>G
ENST00000262407.5:c.3061-220A>G ENSP00000262407.5:n.3061-220A>G
ENST00000587295.5:c.254-220A>G
ENST00000588098.1:c.38-220A>G
NM_000419.3:c.3061-220A>G , LRG_479t1:c.3061-220A>G NP_000410.2:n.3061-220A>G
XM_011524749.1:c.2959-220A>G XP_011523051.1:n.2959-220A>G
XM_011524750.1:c.2944-220A>G XP_011523052.1:n.2944-220A>G
NM_000419.4:c.3061-220A>G NP_000410.2:n.3061-220A>G
NM_000419.5:c.3061-220A>G MANE Select NP_000410.2:n.3061-220A>G
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