Canonical Allele Identifier: CA368054118
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87452987A>T , CM000669.2:g.87452987A>T GRCh38
NC_000007.13:g.87082303A>T , CM000669.1:g.87082303A>T GRCh37
NC_000007.12:g.86920239A>T NCBI36
NG_007118.1:g.32446T>A
NG_007118.2:g.32446T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.493T>A ENSP00000352135.3:p.Phe165Ile
ENST00000643670.1:c.436T>A ENSP00000496629.1:p.Phe146Ile
ENST00000644106.1:c.493T>A ENSP00000493477.1:p.Phe165Ile
ENST00000649586.2:c.493T>A MANE Select ENSP00000496956.2:p.Phe165Ile
ENST00000265723.8:c.493T>A ENSP00000265723.4:p.Phe165Ile
ENST00000358400.7:c.493T>A ENSP00000351172.3:p.Phe165Ile
ENST00000359206.7:c.493T>A ENSP00000352135.3:p.Phe165Ile
ENST00000453593.5:c.493T>A ENSP00000392983.1:p.Phe165Ile
ENST00000473795.1:n.500T>A
NM_000443.3:c.493T>A NP_000434.1:p.Phe165Ile
NM_018849.2:c.493T>A NP_061337.1:p.Phe165Ile
NM_018850.2:c.493T>A NP_061338.1:p.Phe165Ile
XM_011516308.1:c.493T>A XP_011514610.1:p.Phe165Ile
XM_011516309.1:c.493T>A XP_011514611.1:p.Phe165Ile
XM_011516310.1:c.493T>A XP_011514612.1:p.Phe165Ile
XM_011516311.1:c.493T>A XP_011514613.1:p.Phe165Ile
XM_011516312.1:c.493T>A XP_011514614.1:p.Phe165Ile
XM_011516313.1:c.493T>A XP_011514615.1:p.Phe165Ile
XM_011516314.1:c.514T>A XP_011514616.1:p.Phe172Ile
XM_011516315.1:c.-91T>A XP_011514617.1:n.-91T>A
XR_927478.1:n.589T>A
XM_011516308.3:c.763T>A XP_011514610.3:p.Phe255Ile
XM_011516309.3:c.763T>A XP_011514611.3:p.Phe255Ile
XM_011516310.3:c.763T>A XP_011514612.3:p.Phe255Ile
XM_011516311.3:c.763T>A XP_011514613.3:p.Phe255Ile
XM_011516312.3:c.763T>A XP_011514614.3:p.Phe255Ile
XM_011516313.3:c.763T>A XP_011514615.2:p.Phe255Ile
XM_011516315.3:c.-91T>A XP_011514617.2:n.-91T>A
XM_017012323.2:c.493T>A XP_016867812.1:p.Phe165Ile
XR_001744809.2:n.1264T>A
XR_001744810.2:n.1259T>A
NM_000443.4:c.493T>A MANE Select NP_000434.1:p.Phe165Ile
NM_018849.3:c.493T>A NP_061337.1:p.Phe165Ile
NM_018850.3:c.493T>A NP_061338.1:p.Phe165Ile