Canonical Allele Identifier: CA2739546781
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44380812T>G , CM000679.2:g.44380812T>G GRCh38
NC_000017.10:g.42458180T>G , CM000679.1:g.42458180T>G GRCh37
NC_000017.9:g.39813706T>G NCBI36
NG_008331.1:g.13694A>C , LRG_479:g.13694A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1393+67A>C MANE Select ENSP00000262407.5:n.1393+67A>C
ENST00000648408.1:c.824+67A>C
ENST00000262407.5:c.1393+67A>C ENSP00000262407.5:n.1393+67A>C
ENST00000592226.5:n.700A>C
ENST00000592462.5:n.188+67A>C
NM_000419.3:c.1393+67A>C , LRG_479t1:c.1393+67A>C NP_000410.2:n.1393+67A>C
XM_011524749.1:c.1393+67A>C XP_011523051.1:n.1393+67A>C
XM_011524750.1:c.1393+67A>C XP_011523052.1:n.1393+67A>C
NM_000419.4:c.1393+67A>C NP_000410.2:n.1393+67A>C
NM_000419.5:c.1393+67A>C MANE Select NP_000410.2:n.1393+67A>C
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