Canonical Allele Identifier: CA402550742

Gene: ATP8B1

Linked Data

• MyVariant Identifiers: chr18:g.55373801T>G (hg19) ; chr18:g.57706569T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57706569T>G , CM000680.2:g.57706569T>G	GRCh38
NC_000018.9:g.55373801T>G , CM000680.1:g.55373801T>G	GRCh37
NC_000018.8:g.53524799T>G	NCBI36
NG_007148.2:g.101527A>C
NG_007148.3:g.102254A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642462.1:c.200A>C	ENSP00000494712.1:p.Lys67Thr
ENST00000648039.1:c.200A>C	ENSP00000497863.1:p.Lys67Thr
ENST00000648467.1:c.147A>C
ENST00000648908.2:c.200A>C MANE Select	ENSP00000497896.1:p.Lys67Thr
ENST00000283684.8:c.200A>C	ENSP00000283684.4:p.Lys67Thr
ENST00000536015.5:c.200A>C	ENSP00000445359.1:p.Lys67Thr
ENST00000589147.5:n.94A>C
ENST00000591728.1:c.182-1901A>C	ENSP00000467767.1:n.182-1901A>C
NM_005603.4:c.200A>C	NP_005594.1:p.Lys67Thr
XM_006722481.2:c.200A>C	XP_006722544.1:p.Lys67Thr
XM_011526020.1:c.200A>C	XP_011524322.1:p.Lys67Thr
XM_011526021.1:c.200A>C	XP_011524323.1:p.Lys67Thr
XM_011526022.1:c.200A>C	XP_011524324.1:p.Lys67Thr
XM_011526023.1:c.200A>C	XP_011524325.1:p.Lys67Thr
XR_935525.1:n.123+10533T>G
XR_935526.1:n.124-94T>G
NM_005603.6:c.200A>C	NP_005594.2:p.Lys67Thr
XM_006722481.4:c.200A>C	XP_006722544.1:p.Lys67Thr
XM_011526023.3:c.200A>C	XP_011524325.1:p.Lys67Thr
NM_001374385.1:c.200A>C MANE Select	NP_001361314.1:p.Lys67Thr
NM_001374386.1:c.130-1901A>C	NP_001361315.1:n.130-1901A>C