Canonical Allele Identifier: CA1723587166
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402255A= , CM000669.2:g.87402255A= GRCh38
NC_000007.13:g.87031571A= , CM000669.1:g.87031571A= GRCh37
NC_000007.12:g.86869507A= NCBI36
NG_007118.1:g.83178T=
NG_007118.2:g.83178T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3681T= ENSP00000352135.3:p.Ile1227=
ENST00000649586.2:c.3681T= MANE Select ENSP00000496956.2:p.Ile1227=
ENST00000265723.8:c.3702T= ENSP00000265723.4:p.Ile1234=
ENST00000358400.7:c.3540T= ENSP00000351172.3:p.Ile1180=
ENST00000359206.7:c.3681T= ENSP00000352135.3:p.Ile1227=
ENST00000440025.1:c.115T=
ENST00000453593.5:c.3540T= ENSP00000392983.1:p.Ile1180=
ENST00000467983.1:n.293T=
NM_000443.3:c.3681T= NP_000434.1:p.Ile1227=
NM_018849.2:c.3702T= NP_061337.1:p.Ile1234=
NM_018850.2:c.3540T= NP_061338.1:p.Ile1180=
XM_011516308.1:c.3702T= XP_011514610.1:p.Ile1234=
XM_011516309.1:c.3681T= XP_011514611.1:p.Ile1227=
XM_011516310.1:c.3597T= XP_011514612.1:p.Ile1199=
XM_011516311.1:c.3573T= XP_011514613.1:p.Ile1191=
XM_011516312.1:c.3561T= XP_011514614.1:p.Ile1187=
XM_011516313.1:c.3540T= XP_011514615.1:p.Ile1180=
XM_011516314.1:c.3723T= XP_011514616.1:p.Ile1241=
XM_011516315.1:c.3042T= XP_011514617.1:p.Ile1014=
XM_011516308.3:c.3972T= XP_011514610.3:p.Ile1324=
XM_011516309.3:c.3951T= XP_011514611.3:p.Ile1317=
XM_011516310.3:c.3867T= XP_011514612.3:p.Ile1289=
XM_011516311.3:c.3843T= XP_011514613.3:p.Ile1281=
XM_011516312.3:c.3831T= XP_011514614.3:p.Ile1277=
XM_011516313.3:c.3810T= XP_011514615.2:p.Ile1270=
XM_011516315.3:c.3042T= XP_011514617.2:p.Ile1014=
XM_017012323.2:c.3702T= XP_016867812.1:p.Ile1234=
XR_001744809.2:n.4210T=
NM_000443.4:c.3681T= MANE Select NP_000434.1:p.Ile1227=
NM_018849.3:c.3702T= NP_061337.1:p.Ile1234=
NM_018850.3:c.3540T= NP_061338.1:p.Ile1180=