Canonical Allele Identifier: CA2638215550
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375724_44375725dup , CM000679.2:g.44375724_44375725dup GRCh38
NC_000017.10:g.42453092_42453093dup , CM000679.1:g.42453092_42453093dup GRCh37
NC_000017.9:g.39808618_39808619dup NCBI36
NG_008331.1:g.18786_18787dup , LRG_479:g.18786_18787dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2602-4_2602-3dup MANE Select ENSP00000262407.5:n.2602-4_2602-3dup
ENST00000648408.1:c.2033-4_2033-3dup
ENST00000262407.5:c.2602-4_2602-3dup ENSP00000262407.5:n.2602-4_2602-3dup
ENST00000587295.5:c.253+113_253+114dup
ENST00000592462.5:n.1397-4_1397-3dup
NM_000419.3:c.2602-4_2602-3dup , LRG_479t1:c.2602-4_2602-3dup NP_000410.2:n.2602-4_2602-3dup
XM_011524749.1:c.2602-4_2602-3dup XP_011523051.1:n.2602-4_2602-3dup
XM_011524750.1:c.2602-4_2602-3dup XP_011523052.1:n.2602-4_2602-3dup
NM_000419.4:c.2602-4_2602-3dup NP_000410.2:n.2602-4_2602-3dup
NM_000419.5:c.2602-4_2602-3dup MANE Select NP_000410.2:n.2602-4_2602-3dup