Canonical Allele Identifier: CA1723587186
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402262G= , CM000669.2:g.87402262G= GRCh38
NC_000007.13:g.87031578G= , CM000669.1:g.87031578G= GRCh37
NC_000007.12:g.86869514G= NCBI36
NG_007118.1:g.83171C=
NG_007118.2:g.83171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3674C= ENSP00000352135.3:p.Thr1225=
ENST00000649586.2:c.3674C= MANE Select ENSP00000496956.2:p.Thr1225=
ENST00000265723.8:c.3695C= ENSP00000265723.4:p.Thr1232=
ENST00000358400.7:c.3533C= ENSP00000351172.3:p.Thr1178=
ENST00000359206.7:c.3674C= ENSP00000352135.3:p.Thr1225=
ENST00000440025.1:c.108C=
ENST00000453593.5:c.3533C= ENSP00000392983.1:p.Thr1178=
ENST00000467983.1:n.286C=
NM_000443.3:c.3674C= NP_000434.1:p.Thr1225=
NM_018849.2:c.3695C= NP_061337.1:p.Thr1232=
NM_018850.2:c.3533C= NP_061338.1:p.Thr1178=
XM_011516308.1:c.3695C= XP_011514610.1:p.Thr1232=
XM_011516309.1:c.3674C= XP_011514611.1:p.Thr1225=
XM_011516310.1:c.3590C= XP_011514612.1:p.Thr1197=
XM_011516311.1:c.3566C= XP_011514613.1:p.Thr1189=
XM_011516312.1:c.3554C= XP_011514614.1:p.Thr1185=
XM_011516313.1:c.3533C= XP_011514615.1:p.Thr1178=
XM_011516314.1:c.3716C= XP_011514616.1:p.Thr1239=
XM_011516315.1:c.3035C= XP_011514617.1:p.Thr1012=
XM_011516308.3:c.3965C= XP_011514610.3:p.Thr1322=
XM_011516309.3:c.3944C= XP_011514611.3:p.Thr1315=
XM_011516310.3:c.3860C= XP_011514612.3:p.Thr1287=
XM_011516311.3:c.3836C= XP_011514613.3:p.Thr1279=
XM_011516312.3:c.3824C= XP_011514614.3:p.Thr1275=
XM_011516313.3:c.3803C= XP_011514615.2:p.Thr1268=
XM_011516315.3:c.3035C= XP_011514617.2:p.Thr1012=
XM_017012323.2:c.3695C= XP_016867812.1:p.Thr1232=
XR_001744809.2:n.4203C=
NM_000443.4:c.3674C= MANE Select NP_000434.1:p.Thr1225=
NM_018849.3:c.3695C= NP_061337.1:p.Thr1232=
NM_018850.3:c.3533C= NP_061338.1:p.Thr1178=