Canonical Allele Identifier: CA2306111613

Gene: ATP8B1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57694541G= , CM000680.2:g.57694541G=	GRCh38
NC_000018.9:g.55361773G= , CM000680.1:g.55361773G=	GRCh37
NC_000018.8:g.53512771G=	NCBI36
NG_007148.2:g.113555C=
NG_007148.3:g.114282C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.1029+41C=	ENSP00000494712.1:n.1029+41C=
ENST00000648039.1:c.1029+41C=	ENSP00000497863.1:n.1029+41C=
ENST00000648467.1:c.862+41C=
ENST00000648908.2:c.1029+41C= MANE Select	ENSP00000497896.1:n.1029+41C=
ENST00000283684.8:c.1029+41C=	ENSP00000283684.4:n.1029+41C=
ENST00000536015.5:c.1029+41C=	ENSP00000445359.1:n.1029+41C=
NM_005603.4:c.1029+41C=	NP_005594.1:n.1029+41C=
XM_006722481.2:c.1029+41C=	XP_006722544.1:n.1029+41C=
XM_011526020.1:c.1029+41C=	XP_011524322.1:n.1029+41C=
XM_011526021.1:c.1029+41C=	XP_011524323.1:n.1029+41C=
XM_011526022.1:c.1029+41C=	XP_011524324.1:n.1029+41C=
XM_011526023.1:c.915+41C=	XP_011524325.1:n.915+41C=
XM_011526024.1:c.309+41C=	XP_011524326.1:n.309+41C=
XR_935525.1:n.32-1404G=
XR_935526.1:n.32-1404G=
NM_005603.6:c.1029+41C=	NP_005594.2:n.1029+41C=
XM_006722481.4:c.1029+41C=	XP_006722544.1:n.1029+41C=
XM_011526023.3:c.915+41C=	XP_011524325.1:n.915+41C=
NM_001374385.1:c.1029+41C= MANE Select	NP_001361314.1:n.1029+41C=
NM_001374386.1:c.879+41C=	NP_001361315.1:n.879+41C=