Canonical Allele Identifier: CA368061133
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87417347T>A , CM000669.2:g.87417347T>A GRCh38
NC_000007.13:g.87046663T>A , CM000669.1:g.87046663T>A GRCh37
NC_000007.12:g.86884599T>A NCBI36
NG_007118.1:g.68086A>T
NG_007118.2:g.68086A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.2647A>T ENSP00000352135.3:p.Lys883Ter
ENST00000649586.2:c.2647A>T MANE Select ENSP00000496956.2:p.Lys883Ter
ENST00000265723.8:c.2647A>T ENSP00000265723.4:p.Lys883Ter
ENST00000358400.7:c.2647A>T ENSP00000351172.3:p.Lys883Ter
ENST00000359206.7:c.2647A>T ENSP00000352135.3:p.Lys883Ter
ENST00000453593.5:c.2647A>T ENSP00000392983.1:p.Lys883Ter
NM_000443.3:c.2647A>T NP_000434.1:p.Lys883Ter
NM_018849.2:c.2647A>T NP_061337.1:p.Lys883Ter
NM_018850.2:c.2647A>T NP_061338.1:p.Lys883Ter
XM_011516308.1:c.2647A>T XP_011514610.1:p.Lys883Ter
XM_011516309.1:c.2647A>T XP_011514611.1:p.Lys883Ter
XM_011516310.1:c.2542A>T XP_011514612.1:p.Lys848Ter
XM_011516311.1:c.2647A>T XP_011514613.1:p.Lys883Ter
XM_011516312.1:c.2647A>T XP_011514614.1:p.Lys883Ter
XM_011516313.1:c.2647A>T XP_011514615.1:p.Lys883Ter
XM_011516314.1:c.2668A>T XP_011514616.1:p.Lys890Ter
XM_011516315.1:c.1987A>T XP_011514617.1:p.Lys663Ter
XR_927478.1:n.2743A>T
XM_011516308.3:c.2917A>T XP_011514610.3:p.Lys973Ter
XM_011516309.3:c.2917A>T XP_011514611.3:p.Lys973Ter
XM_011516310.3:c.2812A>T XP_011514612.3:p.Lys938Ter
XM_011516311.3:c.2917A>T XP_011514613.3:p.Lys973Ter
XM_011516312.3:c.2917A>T XP_011514614.3:p.Lys973Ter
XM_011516313.3:c.2917A>T XP_011514615.2:p.Lys973Ter
XM_011516315.3:c.1987A>T XP_011514617.2:p.Lys663Ter
XM_017012323.2:c.2647A>T XP_016867812.1:p.Lys883Ter
XR_001744809.2:n.3418A>T
NM_000443.4:c.2647A>T MANE Select NP_000434.1:p.Lys883Ter
NM_018849.3:c.2647A>T NP_061337.1:p.Lys883Ter
NM_018850.3:c.2647A>T NP_061338.1:p.Lys883Ter