Canonical Allele Identifier: CA1302155993
Gene: ITGB6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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