Canonical Allele Identifier: CA504021304

Gene: ATP8B1

Linked Data

• MyVariant Identifiers: chr18:g.55342208T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674976T>A , CM000680.2:g.57674976T>A	GRCh38
NC_000018.9:g.55342208T>A , CM000680.1:g.55342208T>A	GRCh37
NC_000018.8:g.53493206T>A	NCBI36
NG_007148.2:g.133120A>T
NG_007148.3:g.133847A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.1677A>T	ENSP00000494712.1:p.Val559=
ENST00000648039.1:c.1677A>T	ENSP00000497863.1:p.Val559=
ENST00000648467.1:c.1542A>T
ENST00000648908.2:c.1677A>T MANE Select	ENSP00000497896.1:p.Val559=
ENST00000283684.8:c.1677A>T	ENSP00000283684.4:p.Val559=
ENST00000536015.5:c.1677A>T	ENSP00000445359.1:p.Val559=
NM_005603.4:c.1677A>T	NP_005594.1:p.Val559=
XM_006722481.2:c.1677A>T	XP_006722544.1:p.Val559=
XM_011526020.1:c.1677A>T	XP_011524322.1:p.Val559=
XM_011526021.1:c.1677A>T	XP_011524323.1:p.Val559=
XM_011526022.1:c.1677A>T	XP_011524324.1:p.Val559=
XM_011526023.1:c.1563A>T	XP_011524325.1:p.Val521=
XM_011526024.1:c.957A>T	XP_011524326.1:p.Val319=
NM_005603.6:c.1677A>T	NP_005594.2:p.Val559=
XM_006722481.4:c.1677A>T	XP_006722544.1:p.Val559=
XM_011526023.3:c.1563A>T	XP_011524325.1:p.Val521=
NM_001374385.1:c.1677A>T MANE Select	NP_001361314.1:p.Val559=
NM_001374386.1:c.1527A>T	NP_001361315.1:p.Val509=