Canonical Allele Identifier: CA402560902

Gene: ATP8B1

Linked Data

• gnomAD v4: 18-57674894-T-C
• MyVariant Identifiers: chr18:g.55342126T>C (hg19) ; chr18:g.57674894T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674894T>C , CM000680.2:g.57674894T>C	GRCh38
NC_000018.9:g.55342126T>C , CM000680.1:g.55342126T>C	GRCh37
NC_000018.8:g.53493124T>C	NCBI36
NG_007148.2:g.133202A>G
NG_007148.3:g.133929A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642462.1:c.1759A>G	ENSP00000494712.1:p.Thr587Ala
ENST00000648039.1:c.1759A>G	ENSP00000497863.1:p.Thr587Ala
ENST00000648467.1:c.1624A>G
ENST00000648908.2:c.1759A>G MANE Select	ENSP00000497896.1:p.Thr587Ala
ENST00000283684.8:c.1759A>G	ENSP00000283684.4:p.Thr587Ala
ENST00000536015.5:c.1759A>G	ENSP00000445359.1:p.Thr587Ala
NM_005603.4:c.1759A>G	NP_005594.1:p.Thr587Ala
XM_006722481.2:c.1759A>G	XP_006722544.1:p.Thr587Ala
XM_011526020.1:c.1759A>G	XP_011524322.1:p.Thr587Ala
XM_011526021.1:c.1759A>G	XP_011524323.1:p.Thr587Ala
XM_011526022.1:c.1759A>G	XP_011524324.1:p.Thr587Ala
XM_011526023.1:c.1645A>G	XP_011524325.1:p.Thr549Ala
XM_011526024.1:c.1039A>G	XP_011524326.1:p.Thr347Ala
NM_005603.6:c.1759A>G	NP_005594.2:p.Thr587Ala
XM_006722481.4:c.1759A>G	XP_006722544.1:p.Thr587Ala
XM_011526023.3:c.1645A>G	XP_011524325.1:p.Thr549Ala
NM_001374385.1:c.1759A>G MANE Select	NP_001361314.1:p.Thr587Ala
NM_001374386.1:c.1609A>G	NP_001361315.1:p.Thr537Ala