Canonical Allele Identifier: CA504021214

Gene: ATP8B1

Linked Data

• MyVariant Identifiers: chr18:g.55342129T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674897T>G , CM000680.2:g.57674897T>G	GRCh38
NC_000018.9:g.55342129T>G , CM000680.1:g.55342129T>G	GRCh37
NC_000018.8:g.53493127T>G	NCBI36
NG_007148.2:g.133199A>C
NG_007148.3:g.133926A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642462.1:c.1756A>C	ENSP00000494712.1:p.Arg586=
ENST00000648039.1:c.1756A>C	ENSP00000497863.1:p.Arg586=
ENST00000648467.1:c.1621A>C
ENST00000648908.2:c.1756A>C MANE Select	ENSP00000497896.1:p.Arg586=
ENST00000283684.8:c.1756A>C	ENSP00000283684.4:p.Arg586=
ENST00000536015.5:c.1756A>C	ENSP00000445359.1:p.Arg586=
NM_005603.4:c.1756A>C	NP_005594.1:p.Arg586=
XM_006722481.2:c.1756A>C	XP_006722544.1:p.Arg586=
XM_011526020.1:c.1756A>C	XP_011524322.1:p.Arg586=
XM_011526021.1:c.1756A>C	XP_011524323.1:p.Arg586=
XM_011526022.1:c.1756A>C	XP_011524324.1:p.Arg586=
XM_011526023.1:c.1642A>C	XP_011524325.1:p.Arg548=
XM_011526024.1:c.1036A>C	XP_011524326.1:p.Arg346=
NM_005603.6:c.1756A>C	NP_005594.2:p.Arg586=
XM_006722481.4:c.1756A>C	XP_006722544.1:p.Arg586=
XM_011526023.3:c.1642A>C	XP_011524325.1:p.Arg548=
NM_001374385.1:c.1756A>C MANE Select	NP_001361314.1:p.Arg586=
NM_001374386.1:c.1606A>C	NP_001361315.1:p.Arg536=