Canonical Allele Identifier: CA1723587209
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402272C= , CM000669.2:g.87402272C= GRCh38
NC_000007.13:g.87031588C= , CM000669.1:g.87031588C= GRCh37
NC_000007.12:g.86869524C= NCBI36
NG_007118.1:g.83161G=
NG_007118.2:g.83161G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3664G= ENSP00000352135.3:p.Glu1222=
ENST00000649586.2:c.3664G= MANE Select ENSP00000496956.2:p.Glu1222=
ENST00000265723.8:c.3685G= ENSP00000265723.4:p.Glu1229=
ENST00000358400.7:c.3523G= ENSP00000351172.3:p.Glu1175=
ENST00000359206.7:c.3664G= ENSP00000352135.3:p.Glu1222=
ENST00000440025.1:c.98G=
ENST00000453593.5:c.3523G= ENSP00000392983.1:p.Glu1175=
ENST00000467983.1:n.276G=
NM_000443.3:c.3664G= NP_000434.1:p.Glu1222=
NM_018849.2:c.3685G= NP_061337.1:p.Glu1229=
NM_018850.2:c.3523G= NP_061338.1:p.Glu1175=
XM_011516308.1:c.3685G= XP_011514610.1:p.Glu1229=
XM_011516309.1:c.3664G= XP_011514611.1:p.Glu1222=
XM_011516310.1:c.3580G= XP_011514612.1:p.Glu1194=
XM_011516311.1:c.3556G= XP_011514613.1:p.Glu1186=
XM_011516312.1:c.3544G= XP_011514614.1:p.Glu1182=
XM_011516313.1:c.3523G= XP_011514615.1:p.Glu1175=
XM_011516314.1:c.3706G= XP_011514616.1:p.Glu1236=
XM_011516315.1:c.3025G= XP_011514617.1:p.Glu1009=
XM_011516308.3:c.3955G= XP_011514610.3:p.Glu1319=
XM_011516309.3:c.3934G= XP_011514611.3:p.Glu1312=
XM_011516310.3:c.3850G= XP_011514612.3:p.Glu1284=
XM_011516311.3:c.3826G= XP_011514613.3:p.Glu1276=
XM_011516312.3:c.3814G= XP_011514614.3:p.Glu1272=
XM_011516313.3:c.3793G= XP_011514615.2:p.Glu1265=
XM_011516315.3:c.3025G= XP_011514617.2:p.Glu1009=
XM_017012323.2:c.3685G= XP_016867812.1:p.Glu1229=
XR_001744809.2:n.4193G=
NM_000443.4:c.3664G= MANE Select NP_000434.1:p.Glu1222=
NM_018849.3:c.3685G= NP_061337.1:p.Glu1229=
NM_018850.3:c.3523G= NP_061338.1:p.Glu1175=