Canonical Allele Identifier: CA11165515

Gene: ITGB6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160108189T>G , CM000664.2:g.160108189T>G	GRCh38
NC_000002.11:g.160964700T>G , CM000664.1:g.160964700T>G	GRCh37
NC_000002.10:g.160672946T>G	NCBI36
NG_042041.1:g.97125A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283249.7:c.2102-344A>C MANE Select	ENSP00000283249.2:n.2102-344A>C
ENST00000283249.6:c.2102-344A>C	ENSP00000283249.2:n.2102-344A>C
ENST00000409583.5:c.*1716-344A>C	ENSP00000386477.1:n.*1716-344A>C
ENST00000409872.1:c.2102-344A>C	ENSP00000386367.1:n.2102-344A>C
ENST00000409967.6:c.1781-344A>C	ENSP00000386828.2:n.1781-344A>C
ENST00000428609.6:c.1976-344A>C	ENSP00000408024.2:n.1976-344A>C
ENST00000475438.1:n.32-344A>C
ENST00000620391.4:c.1817-344A>C	ENSP00000481183.1:n.1817-344A>C
NM_000888.4:c.2102-344A>C	NP_000879.2:n.2102-344A>C
NM_001282353.1:c.2102-344A>C	NP_001269282.1:n.2102-344A>C
NM_001282354.1:c.1817-344A>C	NP_001269283.1:n.1817-344A>C
NM_001282355.1:c.1781-344A>C	NP_001269284.1:n.1781-344A>C
NM_001282388.1:c.1976-344A>C	NP_001269317.1:n.1976-344A>C
NM_001282389.1:c.1883-344A>C	NP_001269318.1:n.1883-344A>C
NM_001282390.1:c.1688-344A>C	NP_001269319.1:n.1688-344A>C
XR_923525.1:n.1039-33474T>G
NM_000888.5:c.2102-344A>C MANE Select	NP_000879.2:n.2102-344A>C
NM_001282353.2:c.2102-344A>C	NP_001269282.1:n.2102-344A>C
NM_001282355.2:c.1781-344A>C	NP_001269284.1:n.1781-344A>C
NM_001282388.2:c.1976-344A>C	NP_001269317.1:n.1976-344A>C
NM_001282389.2:c.1883-344A>C	NP_001269318.1:n.1883-344A>C
NM_001282390.2:c.1688-344A>C	NP_001269319.1:n.1688-344A>C
NM_001282354.2:c.1817-344A>C	NP_001269283.1:n.1817-344A>C