Canonical Allele Identifier: CA1723587185
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402260A= , CM000669.2:g.87402260A= GRCh38
NC_000007.13:g.87031576A= , CM000669.1:g.87031576A= GRCh37
NC_000007.12:g.86869512A= NCBI36
NG_007118.1:g.83173T=
NG_007118.2:g.83173T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3676T= ENSP00000352135.3:p.Cys1226=
ENST00000649586.2:c.3676T= MANE Select ENSP00000496956.2:p.Cys1226=
ENST00000265723.8:c.3697T= ENSP00000265723.4:p.Cys1233=
ENST00000358400.7:c.3535T= ENSP00000351172.3:p.Cys1179=
ENST00000359206.7:c.3676T= ENSP00000352135.3:p.Cys1226=
ENST00000440025.1:c.110T=
ENST00000453593.5:c.3535T= ENSP00000392983.1:p.Cys1179=
ENST00000467983.1:n.288T=
NM_000443.3:c.3676T= NP_000434.1:p.Cys1226=
NM_018849.2:c.3697T= NP_061337.1:p.Cys1233=
NM_018850.2:c.3535T= NP_061338.1:p.Cys1179=
XM_011516308.1:c.3697T= XP_011514610.1:p.Cys1233=
XM_011516309.1:c.3676T= XP_011514611.1:p.Cys1226=
XM_011516310.1:c.3592T= XP_011514612.1:p.Cys1198=
XM_011516311.1:c.3568T= XP_011514613.1:p.Cys1190=
XM_011516312.1:c.3556T= XP_011514614.1:p.Cys1186=
XM_011516313.1:c.3535T= XP_011514615.1:p.Cys1179=
XM_011516314.1:c.3718T= XP_011514616.1:p.Cys1240=
XM_011516315.1:c.3037T= XP_011514617.1:p.Cys1013=
XM_011516308.3:c.3967T= XP_011514610.3:p.Cys1323=
XM_011516309.3:c.3946T= XP_011514611.3:p.Cys1316=
XM_011516310.3:c.3862T= XP_011514612.3:p.Cys1288=
XM_011516311.3:c.3838T= XP_011514613.3:p.Cys1280=
XM_011516312.3:c.3826T= XP_011514614.3:p.Cys1276=
XM_011516313.3:c.3805T= XP_011514615.2:p.Cys1269=
XM_011516315.3:c.3037T= XP_011514617.2:p.Cys1013=
XM_017012323.2:c.3697T= XP_016867812.1:p.Cys1233=
XR_001744809.2:n.4205T=
NM_000443.4:c.3676T= MANE Select NP_000434.1:p.Cys1226=
NM_018849.3:c.3697T= NP_061337.1:p.Cys1233=
NM_018850.3:c.3535T= NP_061338.1:p.Cys1179=