Canonical Allele Identifier: CA2576512584
Gene: ATP8B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57694757T>C , CM000680.2:g.57694757T>C GRCh38
NC_000018.9:g.55361989T>C , CM000680.1:g.55361989T>C GRCh37
NC_000018.8:g.53512987T>C NCBI36
NG_007148.2:g.113339A>G
NG_007148.3:g.114066A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642462.1:c.941-87A>G ENSP00000494712.1:n.941-87A>G
ENST00000648039.1:c.941-87A>G ENSP00000497863.1:n.941-87A>G
ENST00000648467.1:c.774-87A>G
ENST00000648908.2:c.941-87A>G MANE Select ENSP00000497896.1:n.941-87A>G
ENST00000283684.8:c.941-87A>G ENSP00000283684.4:n.941-87A>G
ENST00000536015.5:c.941-87A>G ENSP00000445359.1:n.941-87A>G
NM_005603.4:c.941-87A>G NP_005594.1:n.941-87A>G
XM_006722481.2:c.941-87A>G XP_006722544.1:n.941-87A>G
XM_011526020.1:c.941-87A>G XP_011524322.1:n.941-87A>G
XM_011526021.1:c.941-87A>G XP_011524323.1:n.941-87A>G
XM_011526022.1:c.941-87A>G XP_011524324.1:n.941-87A>G
XM_011526023.1:c.827-87A>G XP_011524325.1:n.827-87A>G
XM_011526024.1:c.221-87A>G XP_011524326.1:n.221-87A>G
XR_935525.1:n.32-1188T>C
XR_935526.1:n.32-1188T>C
NM_005603.6:c.941-87A>G NP_005594.2:n.941-87A>G
XM_006722481.4:c.941-87A>G XP_006722544.1:n.941-87A>G
XM_011526023.3:c.827-87A>G XP_011524325.1:n.827-87A>G
NM_001374385.1:c.941-87A>G MANE Select NP_001361314.1:n.941-87A>G
NM_001374386.1:c.791-87A>G NP_001361315.1:n.791-87A>G