Canonical Allele Identifier: CA2565213604
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375291_44375292del , CM000679.2:g.44375291_44375292del GRCh38
NC_000017.10:g.42452659_42452660del , CM000679.1:g.42452659_42452660del GRCh37
NC_000017.9:g.39808185_39808186del NCBI36
NG_008331.1:g.19215_19216del , LRG_479:g.19215_19216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2728-180_2728-179del MANE Select ENSP00000262407.5:n.2728-180_2728-179del
ENST00000648408.1:c.2159-180_2159-179del
ENST00000262407.5:c.2728-180_2728-179del ENSP00000262407.5:n.2728-180_2728-179del
ENST00000587295.5:c.253+542_253+543del
ENST00000592462.5:n.1822_1823del
NM_000419.3:c.2728-180_2728-179del , LRG_479t1:c.2728-180_2728-179del NP_000410.2:n.2728-180_2728-179del
XM_011524749.1:c.2728-180_2728-179del XP_011523051.1:n.2728-180_2728-179del
XM_011524750.1:c.2728-180_2728-179del XP_011523052.1:n.2728-180_2728-179del
NM_000419.4:c.2728-180_2728-179del NP_000410.2:n.2728-180_2728-179del
NM_000419.5:c.2728-180_2728-179del MANE Select NP_000410.2:n.2728-180_2728-179del