Canonical Allele Identifier: CA456358266

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87046643C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87417327C>A , CM000669.2:g.87417327C>A	GRCh38
NC_000007.13:g.87046643C>A , CM000669.1:g.87046643C>A	GRCh37
NC_000007.12:g.86884579C>A	NCBI36
NG_007118.1:g.68106G>T
NG_007118.2:g.68106G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2667G>T	ENSP00000352135.3:p.Leu889=
ENST00000649586.2:c.2667G>T MANE Select	ENSP00000496956.2:p.Leu889=
ENST00000265723.8:c.2667G>T	ENSP00000265723.4:p.Leu889=
ENST00000358400.7:c.2667G>T	ENSP00000351172.3:p.Leu889=
ENST00000359206.7:c.2667G>T	ENSP00000352135.3:p.Leu889=
ENST00000453593.5:c.2667G>T	ENSP00000392983.1:p.Leu889=
NM_000443.3:c.2667G>T	NP_000434.1:p.Leu889=
NM_018849.2:c.2667G>T	NP_061337.1:p.Leu889=
NM_018850.2:c.2667G>T	NP_061338.1:p.Leu889=
XM_011516308.1:c.2667G>T	XP_011514610.1:p.Leu889=
XM_011516309.1:c.2667G>T	XP_011514611.1:p.Leu889=
XM_011516310.1:c.2562G>T	XP_011514612.1:p.Leu854=
XM_011516311.1:c.2667G>T	XP_011514613.1:p.Leu889=
XM_011516312.1:c.2667G>T	XP_011514614.1:p.Leu889=
XM_011516313.1:c.2667G>T	XP_011514615.1:p.Leu889=
XM_011516314.1:c.2688G>T	XP_011514616.1:p.Leu896=
XM_011516315.1:c.2007G>T	XP_011514617.1:p.Leu669=
XR_927478.1:n.2763G>T
XM_011516308.3:c.2937G>T	XP_011514610.3:p.Leu979=
XM_011516309.3:c.2937G>T	XP_011514611.3:p.Leu979=
XM_011516310.3:c.2832G>T	XP_011514612.3:p.Leu944=
XM_011516311.3:c.2937G>T	XP_011514613.3:p.Leu979=
XM_011516312.3:c.2937G>T	XP_011514614.3:p.Leu979=
XM_011516313.3:c.2937G>T	XP_011514615.2:p.Leu979=
XM_011516315.3:c.2007G>T	XP_011514617.2:p.Leu669=
XM_017012323.2:c.2667G>T	XP_016867812.1:p.Leu889=
XR_001744809.2:n.3438G>T
NM_000443.4:c.2667G>T MANE Select	NP_000434.1:p.Leu889=
NM_018849.3:c.2667G>T	NP_061337.1:p.Leu889=
NM_018850.3:c.2667G>T	NP_061338.1:p.Leu889=