Canonical Allele Identifier: CA8974475
Gene: ATP8B1 HGNC NCBI

Linked Data

dbSNP Id: rs752703482

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57674846T>C , CM000680.2:g.57674846T>C GRCh38
NC_000018.9:g.55342078T>C , CM000680.1:g.55342078T>C GRCh37
NC_000018.8:g.53493076T>C NCBI36
NG_007148.2:g.133250A>G
NG_007148.3:g.133977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642462.1:c.1807A>G ENSP00000494712.1:p.Met603Val
ENST00000648039.1:c.1807A>G ENSP00000497863.1:p.Met603Val
ENST00000648467.1:c.1672A>G
ENST00000648908.2:c.1807A>G MANE Select ENSP00000497896.1:p.Met603Val
ENST00000283684.8:c.1807A>G ENSP00000283684.4:p.Met603Val
ENST00000536015.5:c.1807A>G ENSP00000445359.1:p.Met603Val
NM_005603.4:c.1807A>G NP_005594.1:p.Met603Val
XM_006722481.2:c.1807A>G XP_006722544.1:p.Met603Val
XM_011526020.1:c.1807A>G XP_011524322.1:p.Met603Val
XM_011526021.1:c.1807A>G XP_011524323.1:p.Met603Val
XM_011526022.1:c.1807A>G XP_011524324.1:p.Met603Val
XM_011526023.1:c.1693A>G XP_011524325.1:p.Met565Val
XM_011526024.1:c.1087A>G XP_011524326.1:p.Met363Val
NM_005603.6:c.1807A>G NP_005594.2:p.Met603Val
XM_006722481.4:c.1807A>G XP_006722544.1:p.Met603Val
XM_011526023.3:c.1693A>G XP_011524325.1:p.Met565Val
NM_001374385.1:c.1807A>G MANE Select NP_001361314.1:p.Met603Val
NM_001374386.1:c.1657A>G NP_001361315.1:p.Met553Val