Canonical Allele Identifier: CA368060576
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87411952A>T , CM000669.2:g.87411952A>T GRCh38
NC_000007.13:g.87041268A>T , CM000669.1:g.87041268A>T GRCh37
NC_000007.12:g.86879204A>T NCBI36
NG_007118.1:g.73481T>A
NG_007118.2:g.73481T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359206.8:c.2865T>A ENSP00000352135.3:p.Cys955Ter
ENST00000649586.2:c.2865T>A MANE Select ENSP00000496956.2:p.Cys955Ter
ENST00000265723.8:c.2865T>A ENSP00000265723.4:p.Cys955Ter
ENST00000358400.7:c.2783+1665T>A ENSP00000351172.3:n.2783+1665T>A
ENST00000359206.7:c.2865T>A ENSP00000352135.3:p.Cys955Ter
ENST00000453593.5:c.2783+1665T>A ENSP00000392983.1:n.2783+1665T>A
NM_000443.3:c.2865T>A NP_000434.1:p.Cys955Ter
NM_018849.2:c.2865T>A NP_061337.1:p.Cys955Ter
NM_018850.2:c.2783+1665T>A NP_061338.1:n.2783+1665T>A
XM_011516308.1:c.2865T>A XP_011514610.1:p.Cys955Ter
XM_011516309.1:c.2865T>A XP_011514611.1:p.Cys955Ter
XM_011516310.1:c.2760T>A XP_011514612.1:p.Cys920Ter
XM_011516311.1:c.2784-48T>A XP_011514613.1:n.2784-48T>A
XM_011516312.1:c.2783+1665T>A XP_011514614.1:n.2783+1665T>A
XM_011516313.1:c.2783+1665T>A XP_011514615.1:n.2783+1665T>A
XM_011516314.1:c.2886T>A XP_011514616.1:p.Cys962Ter
XM_011516315.1:c.2205T>A XP_011514617.1:p.Cys735Ter
XR_927478.1:n.2779-2560T>A
XM_011516308.3:c.3135T>A XP_011514610.3:p.Cys1045Ter
XM_011516309.3:c.3135T>A XP_011514611.3:p.Cys1045Ter
XM_011516310.3:c.3030T>A XP_011514612.3:p.Cys1010Ter
XM_011516311.3:c.3054-48T>A XP_011514613.3:n.3054-48T>A
XM_011516312.3:c.3053+1665T>A XP_011514614.3:n.3053+1665T>A
XM_011516313.3:c.3053+1665T>A XP_011514615.2:n.3053+1665T>A
XM_011516315.3:c.2205T>A XP_011514617.2:p.Cys735Ter
XM_017012323.2:c.2865T>A XP_016867812.1:p.Cys955Ter
XR_001744809.2:n.3454-2560T>A
NM_000443.4:c.2865T>A MANE Select NP_000434.1:p.Cys955Ter
NM_018849.3:c.2865T>A NP_061337.1:p.Cys955Ter
NM_018850.3:c.2783+1665T>A NP_061338.1:n.2783+1665T>A