Canonical Allele Identifier: CA456348188

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87053342A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87424026A>G , CM000669.2:g.87424026A>G	GRCh38
NC_000007.13:g.87053342A>G , CM000669.1:g.87053342A>G	GRCh37
NC_000007.12:g.86891278A>G	NCBI36
NG_007118.1:g.61407T>C
NG_007118.2:g.61407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2091T>C	ENSP00000352135.3:p.Phe697=
ENST00000643670.1:c.2107T>C	ENSP00000496629.1:n.2107T>C
ENST00000649586.2:c.2091T>C MANE Select	ENSP00000496956.2:p.Phe697=
ENST00000265723.8:c.2091T>C	ENSP00000265723.4:p.Phe697=
ENST00000358400.7:c.2091T>C	ENSP00000351172.3:p.Phe697=
ENST00000359206.7:c.2091T>C	ENSP00000352135.3:p.Phe697=
ENST00000453593.5:c.2091T>C	ENSP00000392983.1:p.Phe697=
ENST00000469770.1:n.295T>C
NM_000443.3:c.2091T>C	NP_000434.1:p.Phe697=
NM_018849.2:c.2091T>C	NP_061337.1:p.Phe697=
NM_018850.2:c.2091T>C	NP_061338.1:p.Phe697=
XM_011516308.1:c.2091T>C	XP_011514610.1:p.Phe697=
XM_011516309.1:c.2091T>C	XP_011514611.1:p.Phe697=
XM_011516310.1:c.2091T>C	XP_011514612.1:p.Phe697=
XM_011516311.1:c.2091T>C	XP_011514613.1:p.Phe697=
XM_011516312.1:c.2091T>C	XP_011514614.1:p.Phe697=
XM_011516313.1:c.2091T>C	XP_011514615.1:p.Phe697=
XM_011516314.1:c.2112T>C	XP_011514616.1:p.Phe704=
XM_011516315.1:c.1431T>C	XP_011514617.1:p.Phe477=
XR_927478.1:n.2187T>C
XM_011516308.3:c.2361T>C	XP_011514610.3:p.Phe787=
XM_011516309.3:c.2361T>C	XP_011514611.3:p.Phe787=
XM_011516310.3:c.2361T>C	XP_011514612.3:p.Phe787=
XM_011516311.3:c.2361T>C	XP_011514613.3:p.Phe787=
XM_011516312.3:c.2361T>C	XP_011514614.3:p.Phe787=
XM_011516313.3:c.2361T>C	XP_011514615.2:p.Phe787=
XM_011516315.3:c.1431T>C	XP_011514617.2:p.Phe477=
XM_017012323.2:c.2091T>C	XP_016867812.1:p.Phe697=
XR_001744809.2:n.2862T>C
XR_001744810.2:n.2857T>C
NM_000443.4:c.2091T>C MANE Select	NP_000434.1:p.Phe697=
NM_018849.3:c.2091T>C	NP_061337.1:p.Phe697=
NM_018850.3:c.2091T>C	NP_061338.1:p.Phe697=