Canonical Allele Identifier: CA1723587162
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402242G= , CM000669.2:g.87402242G= GRCh38
NC_000007.13:g.87031558G= , CM000669.1:g.87031558G= GRCh37
NC_000007.12:g.86869494G= NCBI36
NG_007118.1:g.83191C=
NG_007118.2:g.83191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3694C= ENSP00000352135.3:p.Arg1232=
ENST00000649586.2:c.3694C= MANE Select ENSP00000496956.2:p.Arg1232=
ENST00000265723.8:c.3715C= ENSP00000265723.4:p.Arg1239=
ENST00000358400.7:c.3553C= ENSP00000351172.3:p.Arg1185=
ENST00000359206.7:c.3694C= ENSP00000352135.3:p.Arg1232=
ENST00000440025.1:c.128C=
ENST00000453593.5:c.3553C= ENSP00000392983.1:p.Arg1185=
ENST00000467983.1:n.306C=
NM_000443.3:c.3694C= NP_000434.1:p.Arg1232=
NM_018849.2:c.3715C= NP_061337.1:p.Arg1239=
NM_018850.2:c.3553C= NP_061338.1:p.Arg1185=
XM_011516308.1:c.3715C= XP_011514610.1:p.Arg1239=
XM_011516309.1:c.3694C= XP_011514611.1:p.Arg1232=
XM_011516310.1:c.3610C= XP_011514612.1:p.Arg1204=
XM_011516311.1:c.3586C= XP_011514613.1:p.Arg1196=
XM_011516312.1:c.3574C= XP_011514614.1:p.Arg1192=
XM_011516313.1:c.3553C= XP_011514615.1:p.Arg1185=
XM_011516314.1:c.3736C= XP_011514616.1:p.Arg1246=
XM_011516315.1:c.3055C= XP_011514617.1:p.Arg1019=
XM_011516308.3:c.3985C= XP_011514610.3:p.Arg1329=
XM_011516309.3:c.3964C= XP_011514611.3:p.Arg1322=
XM_011516310.3:c.3880C= XP_011514612.3:p.Arg1294=
XM_011516311.3:c.3856C= XP_011514613.3:p.Arg1286=
XM_011516312.3:c.3844C= XP_011514614.3:p.Arg1282=
XM_011516313.3:c.3823C= XP_011514615.2:p.Arg1275=
XM_011516315.3:c.3055C= XP_011514617.2:p.Arg1019=
XM_017012323.2:c.3715C= XP_016867812.1:p.Arg1239=
XR_001744809.2:n.4223C=
NM_000443.4:c.3694C= MANE Select NP_000434.1:p.Arg1232=
NM_018849.3:c.3715C= NP_061337.1:p.Arg1239=
NM_018850.3:c.3553C= NP_061338.1:p.Arg1185=