Canonical Allele Identifier: CA1723573166
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87411965G= , CM000669.2:g.87411965G= GRCh38
NC_000007.13:g.87041281G= , CM000669.1:g.87041281G= GRCh37
NC_000007.12:g.86879217G= NCBI36
NG_007118.1:g.73468C=
NG_007118.2:g.73468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.2852C= ENSP00000352135.3:p.Ser951=
ENST00000649586.2:c.2852C= MANE Select ENSP00000496956.2:p.Ser951=
ENST00000265723.8:c.2852C= ENSP00000265723.4:p.Ser951=
ENST00000358400.7:c.2783+1652C= ENSP00000351172.3:n.2783+1652C=
ENST00000359206.7:c.2852C= ENSP00000352135.3:p.Ser951=
ENST00000453593.5:c.2783+1652C= ENSP00000392983.1:n.2783+1652C=
NM_000443.3:c.2852C= NP_000434.1:p.Ser951=
NM_018849.2:c.2852C= NP_061337.1:p.Ser951=
NM_018850.2:c.2783+1652C= NP_061338.1:n.2783+1652C=
XM_011516308.1:c.2852C= XP_011514610.1:p.Ser951=
XM_011516309.1:c.2852C= XP_011514611.1:p.Ser951=
XM_011516310.1:c.2747C= XP_011514612.1:p.Ser916=
XM_011516311.1:c.2784-61C= XP_011514613.1:n.2784-61C=
XM_011516312.1:c.2783+1652C= XP_011514614.1:n.2783+1652C=
XM_011516313.1:c.2783+1652C= XP_011514615.1:n.2783+1652C=
XM_011516314.1:c.2873C= XP_011514616.1:p.Ser958=
XM_011516315.1:c.2192C= XP_011514617.1:p.Ser731=
XR_927478.1:n.2779-2573C=
XM_011516308.3:c.3122C= XP_011514610.3:p.Ser1041=
XM_011516309.3:c.3122C= XP_011514611.3:p.Ser1041=
XM_011516310.3:c.3017C= XP_011514612.3:p.Ser1006=
XM_011516311.3:c.3054-61C= XP_011514613.3:n.3054-61C=
XM_011516312.3:c.3053+1652C= XP_011514614.3:n.3053+1652C=
XM_011516313.3:c.3053+1652C= XP_011514615.2:n.3053+1652C=
XM_011516315.3:c.2192C= XP_011514617.2:p.Ser731=
XM_017012323.2:c.2852C= XP_016867812.1:p.Ser951=
XR_001744809.2:n.3454-2573C=
NM_000443.4:c.2852C= MANE Select NP_000434.1:p.Ser951=
NM_018849.3:c.2852C= NP_061337.1:p.Ser951=
NM_018850.3:c.2783+1652C= NP_061338.1:n.2783+1652C=