Canonical Allele Identifier: CA402555900

Gene: ATP8B1

Linked Data

• MyVariant Identifiers: chr18:g.55336555A>T (hg19) ; chr18:g.57669323A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57669323A>T , CM000680.2:g.57669323A>T	GRCh38
NC_000018.9:g.55336555A>T , CM000680.1:g.55336555A>T	GRCh37
NC_000018.8:g.53487553A>T	NCBI36
NG_007148.2:g.138773T>A
NG_007148.3:g.139500T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.2092T>A	ENSP00000494712.1:p.Leu698Ile
ENST00000648039.1:c.2092T>A	ENSP00000497863.1:p.Leu698Ile
ENST00000648908.2:c.2092T>A MANE Select	ENSP00000497896.1:p.Leu698Ile
ENST00000283684.8:c.2092T>A	ENSP00000283684.4:p.Leu698Ile
ENST00000536015.5:c.2092T>A	ENSP00000445359.1:p.Leu698Ile
NM_005603.4:c.2092T>A	NP_005594.1:p.Leu698Ile
XM_006722481.2:c.2092T>A	XP_006722544.1:p.Leu698Ile
XM_011526020.1:c.2092T>A	XP_011524322.1:p.Leu698Ile
XM_011526021.1:c.2092T>A	XP_011524323.1:p.Leu698Ile
XM_011526022.1:c.2092T>A	XP_011524324.1:p.Leu698Ile
XM_011526023.1:c.1978T>A	XP_011524325.1:p.Leu660Ile
XM_011526024.1:c.1372T>A	XP_011524326.1:p.Leu458Ile
NM_005603.6:c.2092T>A	NP_005594.2:p.Leu698Ile
XM_006722481.4:c.2092T>A	XP_006722544.1:p.Leu698Ile
XM_011526023.3:c.1978T>A	XP_011524325.1:p.Leu660Ile
NM_001374385.1:c.2092T>A MANE Select	NP_001361314.1:p.Leu698Ile
NM_001374386.1:c.1942T>A	NP_001361315.1:p.Leu648Ile