Canonical Allele Identifier: CA2714037614
Gene: ITGB8 HGNC NCBI

Linked Data

dbSNP Id: rs2128134629

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20358227_20358230del , CM000669.2:g.20358227_20358230del GRCh38
NC_000007.13:g.20397850_20397853del , CM000669.1:g.20397850_20397853del GRCh37
NC_000007.12:g.20364375_20364378del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000222573.5:c.128-5410_128-5407del MANE Select ENSP00000222573.3:n.128-5410_128-5407del
ENST00000222573.4:c.128-5410_128-5407del ENSP00000222573.3:n.128-5410_128-5407del
ENST00000478974.1:n.833-5410_833-5407del
ENST00000537992.5:c.-278-5410_-278-5407del ENSP00000441561.1:n.-278-5410_-278-5407de...
NM_002214.2:c.128-5410_128-5407del NP_002205.1:n.128-5410_128-5407del
XM_011515392.1:c.104-4640_104-4637del XP_011513694.1:n.104-4640_104-4637del
XM_011515393.1:c.104-5410_104-5407del XP_011513695.1:n.104-5410_104-5407del
XM_011515394.1:c.95-5410_95-5407del XP_011513696.1:n.95-5410_95-5407del
XM_011515395.1:c.-278-5410_-278-5407del XP_011513697.1:n.-278-5410_-278-5407del
XM_011515396.1:c.-278-5410_-278-5407del XP_011513698.1:n.-278-5410_-278-5407del
XM_011515393.2:c.104-5410_104-5407del XP_011513695.1:n.104-5410_104-5407del
XM_011515394.2:c.95-5410_95-5407del XP_011513696.1:n.95-5410_95-5407del
XM_017012178.1:c.128-5410_128-5407del XP_016867667.1:n.128-5410_128-5407del
XM_017012179.1:c.128-5410_128-5407del XP_016867668.1:n.128-5410_128-5407del
XM_017012180.1:c.-279+2205_-279+2208del XP_016867669.1:n.-279+2205_-279+2208del
XM_017012181.1:c.-278-5410_-278-5407del XP_016867670.1:n.-278-5410_-278-5407del
XM_017012182.1:c.-278-5410_-278-5407del XP_016867671.1:n.-278-5410_-278-5407del
XM_017012183.1:c.-278-5410_-278-5407del XP_016867672.1:n.-278-5410_-278-5407del
NM_002214.3:c.128-5410_128-5407del MANE Select NP_002205.1:n.128-5410_128-5407del