Canonical Allele Identifier: CA402561360

Gene: ATP8B1

Linked Data

• dbSNP Id: rs1259418259
• MyVariant Identifiers: chr18:g.55342179A>T (hg19) ; chr18:g.57674947A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674947A>T , CM000680.2:g.57674947A>T	GRCh38
NC_000018.9:g.55342179A>T , CM000680.1:g.55342179A>T	GRCh37
NC_000018.8:g.53493177A>T	NCBI36
NG_007148.2:g.133149T>A
NG_007148.3:g.133876T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.1706T>A	ENSP00000494712.1:p.Phe569Tyr
ENST00000648039.1:c.1706T>A	ENSP00000497863.1:p.Phe569Tyr
ENST00000648467.1:c.1571T>A
ENST00000648908.2:c.1706T>A MANE Select	ENSP00000497896.1:p.Phe569Tyr
ENST00000283684.8:c.1706T>A	ENSP00000283684.4:p.Phe569Tyr
ENST00000536015.5:c.1706T>A	ENSP00000445359.1:p.Phe569Tyr
NM_005603.4:c.1706T>A	NP_005594.1:p.Phe569Tyr
XM_006722481.2:c.1706T>A	XP_006722544.1:p.Phe569Tyr
XM_011526020.1:c.1706T>A	XP_011524322.1:p.Phe569Tyr
XM_011526021.1:c.1706T>A	XP_011524323.1:p.Phe569Tyr
XM_011526022.1:c.1706T>A	XP_011524324.1:p.Phe569Tyr
XM_011526023.1:c.1592T>A	XP_011524325.1:p.Phe531Tyr
XM_011526024.1:c.986T>A	XP_011524326.1:p.Phe329Tyr
NM_005603.6:c.1706T>A	NP_005594.2:p.Phe569Tyr
XM_006722481.4:c.1706T>A	XP_006722544.1:p.Phe569Tyr
XM_011526023.3:c.1592T>A	XP_011524325.1:p.Phe531Tyr
NM_001374385.1:c.1706T>A MANE Select	NP_001361314.1:p.Phe569Tyr
NM_001374386.1:c.1556T>A	NP_001361315.1:p.Phe519Tyr