Canonical Allele Identifier: CA456348144

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87053282A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87423966A>G , CM000669.2:g.87423966A>G	GRCh38
NC_000007.13:g.87053282A>G , CM000669.1:g.87053282A>G	GRCh37
NC_000007.12:g.86891218A>G	NCBI36
NG_007118.1:g.61467T>C
NG_007118.2:g.61467T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.2151T>C	ENSP00000352135.3:p.Cys717=
ENST00000643670.1:c.2167T>C	ENSP00000496629.1:n.2167T>C
ENST00000649586.2:c.2151T>C MANE Select	ENSP00000496956.2:p.Cys717=
ENST00000265723.8:c.2151T>C	ENSP00000265723.4:p.Cys717=
ENST00000358400.7:c.2151T>C	ENSP00000351172.3:p.Cys717=
ENST00000359206.7:c.2151T>C	ENSP00000352135.3:p.Cys717=
ENST00000453593.5:c.2151T>C	ENSP00000392983.1:p.Cys717=
ENST00000469770.1:n.355T>C
NM_000443.3:c.2151T>C	NP_000434.1:p.Cys717=
NM_018849.2:c.2151T>C	NP_061337.1:p.Cys717=
NM_018850.2:c.2151T>C	NP_061338.1:p.Cys717=
XM_011516308.1:c.2151T>C	XP_011514610.1:p.Cys717=
XM_011516309.1:c.2151T>C	XP_011514611.1:p.Cys717=
XM_011516310.1:c.2151T>C	XP_011514612.1:p.Cys717=
XM_011516311.1:c.2151T>C	XP_011514613.1:p.Cys717=
XM_011516312.1:c.2151T>C	XP_011514614.1:p.Cys717=
XM_011516313.1:c.2151T>C	XP_011514615.1:p.Cys717=
XM_011516314.1:c.2172T>C	XP_011514616.1:p.Cys724=
XM_011516315.1:c.1491T>C	XP_011514617.1:p.Cys497=
XR_927478.1:n.2247T>C
XM_011516308.3:c.2421T>C	XP_011514610.3:p.Cys807=
XM_011516309.3:c.2421T>C	XP_011514611.3:p.Cys807=
XM_011516310.3:c.2421T>C	XP_011514612.3:p.Cys807=
XM_011516311.3:c.2421T>C	XP_011514613.3:p.Cys807=
XM_011516312.3:c.2421T>C	XP_011514614.3:p.Cys807=
XM_011516313.3:c.2421T>C	XP_011514615.2:p.Cys807=
XM_011516315.3:c.1491T>C	XP_011514617.2:p.Cys497=
XM_017012323.2:c.2151T>C	XP_016867812.1:p.Cys717=
XR_001744809.2:n.2922T>C
XR_001744810.2:n.2917T>C
NM_000443.4:c.2151T>C MANE Select	NP_000434.1:p.Cys717=
NM_018849.3:c.2151T>C	NP_061337.1:p.Cys717=
NM_018850.3:c.2151T>C	NP_061338.1:p.Cys717=