Canonical Allele Identifier: CA2576291024
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375696_44375701del , CM000679.2:g.44375696_44375701del GRCh38
NC_000017.10:g.42453064_42453069del , CM000679.1:g.42453064_42453069del GRCh37
NC_000017.9:g.39808590_39808595del NCBI36
NG_008331.1:g.18809_18814del , LRG_479:g.18809_18814del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2621_2626del MANE Select ENSP00000262407.5:p.Ile874_Pro875del
ENST00000648408.1:c.2052_2057del
ENST00000262407.5:c.2621_2626del ENSP00000262407.5:p.Ile874_Pro875del
ENST00000587295.5:c.253+136_253+141del
ENST00000592462.5:n.1416_1421del
NM_000419.3:c.2621_2626del , LRG_479t1:c.2621_2626del NP_000410.2:p.Ile874_Pro875del
XM_011524749.1:c.2621_2626del XP_011523051.1:p.Ile874_Pro875del
XM_011524750.1:c.2621_2626del XP_011523052.1:p.Ile874_Pro875del
NM_000419.4:c.2621_2626del NP_000410.2:p.Ile874_Pro875del
NM_000419.5:c.2621_2626del MANE Select NP_000410.2:p.Ile874_Pro875del