Canonical Allele Identifier: CA1692911544

Gene: ITGB8

Linked Data

• dbSNP Id: rs1785364585

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20358158_20358172del , CM000669.2:g.20358158_20358172del	GRCh38
NC_000007.13:g.20397781_20397795del , CM000669.1:g.20397781_20397795del	GRCh37
NC_000007.12:g.20364306_20364320del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000222573.5:c.128-5479_128-5465del MANE Select	ENSP00000222573.3:n.128-5479_128-5465del
ENST00000222573.4:c.128-5479_128-5465del	ENSP00000222573.3:n.128-5479_128-5465del
ENST00000478974.1:n.833-5479_833-5465del
ENST00000537992.5:c.-278-5479_-278-5465del	ENSP00000441561.1:n.-278-5479_-278-5465del
NM_002214.2:c.128-5479_128-5465del	NP_002205.1:n.128-5479_128-5465del
XM_011515392.1:c.104-4709_104-4695del	XP_011513694.1:n.104-4709_104-4695del
XM_011515393.1:c.104-5479_104-5465del	XP_011513695.1:n.104-5479_104-5465del
XM_011515394.1:c.95-5479_95-5465del	XP_011513696.1:n.95-5479_95-5465del
XM_011515395.1:c.-278-5479_-278-5465del	XP_011513697.1:n.-278-5479_-278-5465del
XM_011515396.1:c.-278-5479_-278-5465del	XP_011513698.1:n.-278-5479_-278-5465del
XM_011515393.2:c.104-5479_104-5465del	XP_011513695.1:n.104-5479_104-5465del
XM_011515394.2:c.95-5479_95-5465del	XP_011513696.1:n.95-5479_95-5465del
XM_017012178.1:c.128-5479_128-5465del	XP_016867667.1:n.128-5479_128-5465del
XM_017012179.1:c.128-5479_128-5465del	XP_016867668.1:n.128-5479_128-5465del
XM_017012180.1:c.-279+2136_-279+2150del	XP_016867669.1:n.-279+2136_-279+2150del
XM_017012181.1:c.-278-5479_-278-5465del	XP_016867670.1:n.-278-5479_-278-5465del
XM_017012182.1:c.-278-5479_-278-5465del	XP_016867671.1:n.-278-5479_-278-5465del
XM_017012183.1:c.-278-5479_-278-5465del	XP_016867672.1:n.-278-5479_-278-5465del
NM_002214.3:c.128-5479_128-5465del MANE Select	NP_002205.1:n.128-5479_128-5465del