Canonical Allele Identifier: CA8974144
Gene: ATP8B1 HGNC NCBI
ATP8B1-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 259820
dbSNP Id: rs12968116

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57655270C>T , CM000680.2:g.57655270C>T GRCh38
NC_000018.9:g.55322502C>T , CM000680.1:g.55322502C>T GRCh37
NC_000018.8:g.53473500C>T NCBI36
NG_007148.2:g.152826G>A
NG_007148.3:g.153553G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000642462.1:c.*87G>A (ATP8B1) ENSP00000494712.1:n.*87G>A
ENST00000648039.1:c.*87G>A (ATP8B1) ENSP00000497863.1:n.*87G>A
ENST00000648908.2:c.2855G>A (ATP8B1) MANE Select ENSP00000497896.1:p.Arg952Gln
ENST00000283684.8:c.2855G>A (ATP8B1) ENSP00000283684.4:p.Arg952Gln
ENST00000536015.5:c.2855G>A (ATP8B1) ENSP00000445359.1:p.Arg952Gln
NM_001242804.1:c.140-12736C>T (ATP8B1-AS1) NP_001229733.1:n.140-12736C>T
NM_005603.4:c.2855G>A (ATP8B1) NP_005594.1:p.Arg952Gln
XM_006722481.2:c.2855G>A (ATP8B1) XP_006722544.1:p.Arg952Gln
XM_011526020.1:c.2855G>A (ATP8B1) XP_011524322.1:p.Arg952Gln
XM_011526021.1:c.2855G>A (ATP8B1) XP_011524323.1:p.Arg952Gln
XM_011526022.1:c.2855G>A (ATP8B1) XP_011524324.1:p.Arg952Gln
XM_011526023.1:c.2741G>A (ATP8B1) XP_011524325.1:p.Arg914Gln
XM_011526024.1:c.2135G>A (ATP8B1) XP_011524326.1:p.Arg712Gln
NM_005603.6:c.2855G>A (ATP8B1) NP_005594.2:p.Arg952Gln
XM_006722481.4:c.2855G>A (ATP8B1) XP_006722544.1:p.Arg952Gln
XM_011526023.3:c.2741G>A (ATP8B1) XP_011524325.1:p.Arg914Gln
NM_001374385.1:c.2855G>A (ATP8B1) MANE Select NP_001361314.1:p.Arg952Gln
NM_001374386.1:c.2705G>A (ATP8B1) NP_001361315.1:p.Arg902Gln
NR_164148.1:n.683-12736C>T (ATP8B1-AS1)