Canonical Allele Identifier: CA2570179317
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44377693C>A , CM000679.2:g.44377693C>A GRCh38
NC_000017.10:g.42455061C>A , CM000679.1:g.42455061C>A GRCh37
NC_000017.9:g.39810587C>A NCBI36
NG_008331.1:g.16813G>T , LRG_479:g.16813G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2187+5G>T MANE Select ENSP00000262407.5:n.2187+5G>T
ENST00000648408.1:c.1618+5G>T
ENST00000262407.5:c.2187+5G>T ENSP00000262407.5:n.2187+5G>T
ENST00000592462.5:n.982+5G>T
NM_000419.3:c.2187+5G>T , LRG_479t1:c.2187+5G>T NP_000410.2:n.2187+5G>T
XM_011524749.1:c.2187+5G>T XP_011523051.1:n.2187+5G>T
XM_011524750.1:c.2187+5G>T XP_011523052.1:n.2187+5G>T
NM_000419.4:c.2187+5G>T NP_000410.2:n.2187+5G>T
NM_000419.5:c.2187+5G>T MANE Select NP_000410.2:n.2187+5G>T
Search 100 bp 5'
Search 100 bp 3'