Canonical Allele Identifier: CA2036867112

Gene: ITGB7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53200654C= , CM000674.2:g.53200654C=	GRCh38
NC_000012.11:g.53594438C= , CM000674.1:g.53594438C=	GRCh37
NC_000012.10:g.51880705C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267082.10:c.-3-208G= MANE Select	ENSP00000267082.4:n.-3-208G=
ENST00000267082.9:c.-3-208G=	ENSP00000267082.4:n.-3-208G=
ENST00000422257.7:c.-3-208G=	ENSP00000408741.3:n.-3-208G=
ENST00000542497.5:c.-3-208G=	ENSP00000437375.1:n.-3-208G=
ENST00000549086.2:c.-3-208G=	ENSP00000446703.2:n.-3-208G=
ENST00000549462.1:n.51-208G=
ENST00000552935.5:c.-3-208G=	ENSP00000456305.1:n.-3-208G=
ENST00000552972.5:c.-3-208G=	ENSP00000450366.1:n.-3-208G=
ENST00000589179.5:n.173+418G=
NM_000889.2:c.-3-208G=	NP_000880.1:n.-3-208G=
NR_104181.1:n.107-208G=
XM_005268851.2:c.-3-208G=	XP_005268908.1:n.-3-208G=
XM_005268852.3:c.-3-208G=	XP_005268909.1:n.-3-208G=
XM_006719376.2:c.-3-208G=	XP_006719439.1:n.-3-208G=
XR_429099.2:n.233-208G=
XM_005268851.4:c.-3-208G=	XP_005268908.1:n.-3-208G=
XM_005268852.5:c.-3-208G=	XP_005268909.1:n.-3-208G=
XM_006719376.4:c.-3-208G=	XP_006719439.1:n.-3-208G=
XR_001748685.2:n.297-208G=
XR_429099.4:n.297-208G=
NM_000889.3:c.-3-208G= MANE Select	NP_000880.1:n.-3-208G=
NR_104181.2:n.51-208G=