Canonical Allele Identifier: CA1302200947

Gene: ITGB6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160199101C>T , CM000664.2:g.160199101C>T	GRCh38
NC_000002.11:g.161055612C>T , CM000664.1:g.161055612C>T	GRCh37
NC_000002.10:g.160763858C>T	NCBI36
NG_042041.1:g.6213G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000888.5:c.141+78G>A MANE Select	NP_000879.2:n.141+78G>A
ENST00000283249.7:c.141+78G>A MANE Select	ENSP00000283249.2:n.141+78G>A
NM_000888.4:c.141+78G>A	NP_000879.2:n.141+78G>A
NM_001282353.1:c.141+78G>A	NP_001269282.1:n.141+78G>A
NM_001282353.2:c.141+78G>A	NP_001269282.1:n.141+78G>A
NM_001282354.1:c.61+902G>A	NP_001269283.1:n.61+902G>A
NM_001282354.2:c.61+902G>A	NP_001269283.1:n.61+902G>A
NM_001282355.1:c.141+78G>A	NP_001269284.1:n.141+78G>A
NM_001282355.2:c.141+78G>A	NP_001269284.1:n.141+78G>A
NM_001282388.1:c.15+902G>A	NP_001269317.1:n.15+902G>A
NM_001282388.2:c.15+902G>A	NP_001269317.1:n.15+902G>A
NM_001282389.1:c.95+78G>A	NP_001269318.1:n.95+78G>A
NM_001282389.2:c.95+78G>A	NP_001269318.1:n.95+78G>A
NM_001282390.1:c.-101+902G>A	NP_001269319.1:n.-101+902G>A
NM_001282390.2:c.-101+902G>A	NP_001269319.1:n.-101+902G>A
ENST00000283249.6:c.141+78G>A	ENSP00000283249.2:n.141+78G>A
ENST00000409583.5:c.141+78G>A	ENSP00000386477.1:n.141+78G>A
ENST00000409872.1:c.141+78G>A	ENSP00000386367.1:n.141+78G>A
ENST00000409967.6:c.141+78G>A	ENSP00000386828.2:n.141+78G>A
ENST00000428609.6:c.15+902G>A	ENSP00000408024.2:n.15+902G>A
ENST00000485635.1:n.462+2035G>A
ENST00000620391.4:c.61+902G>A	ENSP00000481183.1:n.61+902G>A