Canonical Allele Identifier: CA290942942
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs1039891617
MyVariant Identifiers: chr17:g.42449854T>A (hg19) chr17:g.44372486T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372486T>A , CM000679.2:g.44372486T>A GRCh38
NC_000017.10:g.42449854T>A , CM000679.1:g.42449854T>A GRCh37
NC_000017.9:g.39805380T>A NCBI36
NG_008331.1:g.22020A>T , LRG_479:g.22020A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-63A>T MANE Select ENSP00000262407.5:n.3061-63A>T
ENST00000648408.1:c.2375-63A>T
ENST00000262407.5:c.3061-63A>T ENSP00000262407.5:n.3061-63A>T
ENST00000587295.5:c.254-63A>T
ENST00000588098.1:c.38-63A>T
NM_000419.3:c.3061-63A>T , LRG_479t1:c.3061-63A>T NP_000410.2:n.3061-63A>T
XM_011524749.1:c.2959-63A>T XP_011523051.1:n.2959-63A>T
XM_011524750.1:c.2944-63A>T XP_011523052.1:n.2944-63A>T
NM_000419.4:c.3061-63A>T NP_000410.2:n.3061-63A>T
NM_000419.5:c.3061-63A>T MANE Select NP_000410.2:n.3061-63A>T
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