Canonical Allele Identifier: CA1723579052
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87452880C= , CM000669.2:g.87452880C= GRCh38
NC_000007.13:g.87082196C= , CM000669.1:g.87082196C= GRCh37
NC_000007.12:g.86920132C= NCBI36
NG_007118.1:g.32553G=
NG_007118.2:g.32553G=

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.536+64G= ENSP00000352135.3:n.536+64G=
ENST00000643670.1:c.479+64G= ENSP00000496629.1:n.479+64G=
ENST00000644106.1:c.536+64G= ENSP00000493477.1:n.536+64G=
ENST00000649586.2:c.536+64G= MANE Select ENSP00000496956.2:n.536+64G=
ENST00000265723.8:c.536+64G= ENSP00000265723.4:n.536+64G=
ENST00000358400.7:c.536+64G= ENSP00000351172.3:n.536+64G=
ENST00000359206.7:c.536+64G= ENSP00000352135.3:n.536+64G=
ENST00000453593.5:c.536+64G= ENSP00000392983.1:n.536+64G=
ENST00000473795.1:n.607G=
NM_000443.3:c.536+64G= NP_000434.1:n.536+64G=
NM_018849.2:c.536+64G= NP_061337.1:n.536+64G=
NM_018850.2:c.536+64G= NP_061338.1:n.536+64G=
XM_011516308.1:c.536+64G= XP_011514610.1:n.536+64G=
XM_011516309.1:c.536+64G= XP_011514611.1:n.536+64G=
XM_011516310.1:c.536+64G= XP_011514612.1:n.536+64G=
XM_011516311.1:c.536+64G= XP_011514613.1:n.536+64G=
XM_011516312.1:c.536+64G= XP_011514614.1:n.536+64G=
XM_011516313.1:c.536+64G= XP_011514615.1:n.536+64G=
XM_011516314.1:c.557+64G= XP_011514616.1:n.557+64G=
XM_011516315.1:c.-48+64G= XP_011514617.1:n.-48+64G=
XR_927478.1:n.632+64G=
XM_011516308.3:c.806+64G= XP_011514610.3:n.806+64G=
XM_011516309.3:c.806+64G= XP_011514611.3:n.806+64G=
XM_011516310.3:c.806+64G= XP_011514612.3:n.806+64G=
XM_011516311.3:c.806+64G= XP_011514613.3:n.806+64G=
XM_011516312.3:c.806+64G= XP_011514614.3:n.806+64G=
XM_011516313.3:c.806+64G= XP_011514615.2:n.806+64G=
XM_011516315.3:c.-48+64G= XP_011514617.2:n.-48+64G=
XM_017012323.2:c.536+64G= XP_016867812.1:n.536+64G=
XR_001744809.2:n.1307+64G=
XR_001744810.2:n.1302+64G=
NM_000443.4:c.536+64G= MANE Select NP_000434.1:n.536+64G=
NM_018849.3:c.536+64G= NP_061337.1:n.536+64G=
NM_018850.3:c.536+64G= NP_061338.1:n.536+64G=