Canonical Allele Identifier: CA1723573154
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87411962T= , CM000669.2:g.87411962T= GRCh38
NC_000007.13:g.87041278T= , CM000669.1:g.87041278T= GRCh37
NC_000007.12:g.86879214T= NCBI36
NG_007118.1:g.73471A=
NG_007118.2:g.73471A=

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.2855A= ENSP00000352135.3:p.Tyr952=
ENST00000649586.2:c.2855A= MANE Select ENSP00000496956.2:p.Tyr952=
ENST00000265723.8:c.2855A= ENSP00000265723.4:p.Tyr952=
ENST00000358400.7:c.2783+1655A= ENSP00000351172.3:n.2783+1655A=
ENST00000359206.7:c.2855A= ENSP00000352135.3:p.Tyr952=
ENST00000453593.5:c.2783+1655A= ENSP00000392983.1:n.2783+1655A=
NM_000443.3:c.2855A= NP_000434.1:p.Tyr952=
NM_018849.2:c.2855A= NP_061337.1:p.Tyr952=
NM_018850.2:c.2783+1655A= NP_061338.1:n.2783+1655A=
XM_011516308.1:c.2855A= XP_011514610.1:p.Tyr952=
XM_011516309.1:c.2855A= XP_011514611.1:p.Tyr952=
XM_011516310.1:c.2750A= XP_011514612.1:p.Tyr917=
XM_011516311.1:c.2784-58A= XP_011514613.1:n.2784-58A=
XM_011516312.1:c.2783+1655A= XP_011514614.1:n.2783+1655A=
XM_011516313.1:c.2783+1655A= XP_011514615.1:n.2783+1655A=
XM_011516314.1:c.2876A= XP_011514616.1:p.Tyr959=
XM_011516315.1:c.2195A= XP_011514617.1:p.Tyr732=
XR_927478.1:n.2779-2570A=
XM_011516308.3:c.3125A= XP_011514610.3:p.Tyr1042=
XM_011516309.3:c.3125A= XP_011514611.3:p.Tyr1042=
XM_011516310.3:c.3020A= XP_011514612.3:p.Tyr1007=
XM_011516311.3:c.3054-58A= XP_011514613.3:n.3054-58A=
XM_011516312.3:c.3053+1655A= XP_011514614.3:n.3053+1655A=
XM_011516313.3:c.3053+1655A= XP_011514615.2:n.3053+1655A=
XM_011516315.3:c.2195A= XP_011514617.2:p.Tyr732=
XM_017012323.2:c.2855A= XP_016867812.1:p.Tyr952=
XR_001744809.2:n.3454-2570A=
NM_000443.4:c.2855A= MANE Select NP_000434.1:p.Tyr952=
NM_018849.3:c.2855A= NP_061337.1:p.Tyr952=
NM_018850.3:c.2783+1655A= NP_061338.1:n.2783+1655A=