Canonical Allele Identifier: CA2638216884
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44384209dup , CM000679.2:g.44384209dup GRCh38
NC_000017.10:g.42461577dup , CM000679.1:g.42461577dup GRCh37
NC_000017.9:g.39817103dup NCBI36
NG_008331.1:g.10299dup , LRG_479:g.10299dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.892-69dup MANE Select ENSP00000262407.5:n.892-69dup
ENST00000648408.1:c.323-69dup
ENST00000262407.5:c.892-69dup ENSP00000262407.5:n.892-69dup
ENST00000589645.5:n.343-69dup
ENST00000591990.5:n.437-69dup
ENST00000592075.5:n.261-69dup
ENST00000592226.5:n.132-69dup
ENST00000592253.5:n.400-69dup
NM_000419.3:c.892-69dup , LRG_479t1:c.892-69dup NP_000410.2:n.892-69dup
XM_011524749.1:c.892-69dup XP_011523051.1:n.892-69dup
XM_011524750.1:c.892-69dup XP_011523052.1:n.892-69dup
NM_000419.4:c.892-69dup NP_000410.2:n.892-69dup
NM_000419.5:c.892-69dup MANE Select NP_000410.2:n.892-69dup