Canonical Allele Identifier: CA656365619
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372327_44372328insA , CM000679.2:g.44372327_44372328insA GRCh38
NC_000017.10:g.42449695_42449696insA , CM000679.1:g.42449695_42449696insA GRCh37
NC_000017.9:g.39805221_39805222insA NCBI36
NG_008331.1:g.22178_22179insT , LRG_479:g.22178_22179insT

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.*36_*37insT MANE Select ENSP00000262407.5:n.*36_*37insT
ENST00000648408.1:c.2470_2471insT
ENST00000262407.5:c.*36_*37insT ENSP00000262407.5:n.*36_*37insT
ENST00000587295.5:c.349_350insT
ENST00000588098.1:c.133_134insT
NM_000419.3:c.*36_*37insT , LRG_479t1:c.*36_*37insT NP_000410.2:n.*36_*37insT
XM_011524749.1:c.*36_*37insT XP_011523051.1:n.*36_*37insT
XM_011524750.1:c.*36_*37insT XP_011523052.1:n.*36_*37insT
NM_000419.4:c.*36_*37insT NP_000410.2:n.*36_*37insT
NM_000419.5:c.*36_*37insT MANE Select NP_000410.2:n.*36_*37insT