Canonical Allele Identifier: CA1723587120
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87423899A= , CM000669.2:g.87423899A= GRCh38
NC_000007.13:g.87053215A= , CM000669.1:g.87053215A= GRCh37
NC_000007.12:g.86891151A= NCBI36
NG_007118.1:g.61534T=
NG_007118.2:g.61534T=

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.2211+7T= ENSP00000352135.3:n.2211+7T=
ENST00000643670.1:c.2234T= ENSP00000496629.1:n.2234T=
ENST00000649586.2:c.2211+7T= MANE Select ENSP00000496956.2:n.2211+7T=
ENST00000265723.8:c.2211+7T= ENSP00000265723.4:n.2211+7T=
ENST00000358400.7:c.2211+7T= ENSP00000351172.3:n.2211+7T=
ENST00000359206.7:c.2211+7T= ENSP00000352135.3:n.2211+7T=
ENST00000453593.5:c.2211+7T= ENSP00000392983.1:n.2211+7T=
ENST00000469770.1:n.422T=
NM_000443.3:c.2211+7T= NP_000434.1:n.2211+7T=
NM_018849.2:c.2211+7T= NP_061337.1:n.2211+7T=
NM_018850.2:c.2211+7T= NP_061338.1:n.2211+7T=
XM_011516308.1:c.2211+7T= XP_011514610.1:n.2211+7T=
XM_011516309.1:c.2211+7T= XP_011514611.1:n.2211+7T=
XM_011516310.1:c.2211+7T= XP_011514612.1:n.2211+7T=
XM_011516311.1:c.2211+7T= XP_011514613.1:n.2211+7T=
XM_011516312.1:c.2211+7T= XP_011514614.1:n.2211+7T=
XM_011516313.1:c.2211+7T= XP_011514615.1:n.2211+7T=
XM_011516314.1:c.2232+7T= XP_011514616.1:n.2232+7T=
XM_011516315.1:c.1551+7T= XP_011514617.1:n.1551+7T=
XR_927478.1:n.2307+7T=
XM_011516308.3:c.2481+7T= XP_011514610.3:n.2481+7T=
XM_011516309.3:c.2481+7T= XP_011514611.3:n.2481+7T=
XM_011516310.3:c.2481+7T= XP_011514612.3:n.2481+7T=
XM_011516311.3:c.2481+7T= XP_011514613.3:n.2481+7T=
XM_011516312.3:c.2481+7T= XP_011514614.3:n.2481+7T=
XM_011516313.3:c.2481+7T= XP_011514615.2:n.2481+7T=
XM_011516315.3:c.1551+7T= XP_011514617.2:n.1551+7T=
XM_017012323.2:c.2211+7T= XP_016867812.1:n.2211+7T=
XR_001744809.2:n.2982+7T=
XR_001744810.2:n.2977+7T=
NM_000443.4:c.2211+7T= MANE Select NP_000434.1:n.2211+7T=
NM_018849.3:c.2211+7T= NP_061337.1:n.2211+7T=
NM_018850.3:c.2211+7T= NP_061338.1:n.2211+7T=