Canonical Allele Identifier: CA1692911654

Gene: ITGB8

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20358285G= , CM000669.2:g.20358285G=	GRCh38
NC_000007.13:g.20397908G= , CM000669.1:g.20397908G=	GRCh37
NC_000007.12:g.20364433G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000222573.5:c.128-5352G= MANE Select	ENSP00000222573.3:n.128-5352G=
ENST00000222573.4:c.128-5352G=	ENSP00000222573.3:n.128-5352G=
ENST00000478974.1:n.833-5352G=
ENST00000537992.5:c.-278-5352G=	ENSP00000441561.1:n.-278-5352G=
NM_002214.2:c.128-5352G=	NP_002205.1:n.128-5352G=
XM_011515392.1:c.104-4582G=	XP_011513694.1:n.104-4582G=
XM_011515393.1:c.104-5352G=	XP_011513695.1:n.104-5352G=
XM_011515394.1:c.95-5352G=	XP_011513696.1:n.95-5352G=
XM_011515395.1:c.-278-5352G=	XP_011513697.1:n.-278-5352G=
XM_011515396.1:c.-278-5352G=	XP_011513698.1:n.-278-5352G=
XM_011515393.2:c.104-5352G=	XP_011513695.1:n.104-5352G=
XM_011515394.2:c.95-5352G=	XP_011513696.1:n.95-5352G=
XM_017012178.1:c.128-5352G=	XP_016867667.1:n.128-5352G=
XM_017012179.1:c.128-5352G=	XP_016867668.1:n.128-5352G=
XM_017012180.1:c.-279+2263G=	XP_016867669.1:n.-279+2263G=
XM_017012181.1:c.-278-5352G=	XP_016867670.1:n.-278-5352G=
XM_017012182.1:c.-278-5352G=	XP_016867671.1:n.-278-5352G=
XM_017012183.1:c.-278-5352G=	XP_016867672.1:n.-278-5352G=
NM_002214.3:c.128-5352G= MANE Select	NP_002205.1:n.128-5352G=