Canonical Allele Identifier: CA368048698
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87447119A>G , CM000669.2:g.87447119A>G GRCh38
NC_000007.13:g.87076435A>G , CM000669.1:g.87076435A>G GRCh37
NC_000007.12:g.86914371A>G NCBI36
NG_007118.1:g.38314T>C
NG_007118.2:g.38314T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.920T>C ENSP00000352135.3:p.Leu307Ser
ENST00000643670.1:c.936T>C ENSP00000496629.1:n.936T>C
ENST00000644106.1:c.*457T>C ENSP00000493477.1:n.*457T>C
ENST00000649586.2:c.920T>C MANE Select ENSP00000496956.2:p.Leu307Ser
ENST00000265723.8:c.920T>C ENSP00000265723.4:p.Leu307Ser
ENST00000358400.7:c.920T>C ENSP00000351172.3:p.Leu307Ser
ENST00000359206.7:c.920T>C ENSP00000352135.3:p.Leu307Ser
ENST00000453593.5:c.920T>C ENSP00000392983.1:p.Leu307Ser
NM_000443.3:c.920T>C NP_000434.1:p.Leu307Ser
NM_018849.2:c.920T>C NP_061337.1:p.Leu307Ser
NM_018850.2:c.920T>C NP_061338.1:p.Leu307Ser
XM_011516308.1:c.920T>C XP_011514610.1:p.Leu307Ser
XM_011516309.1:c.920T>C XP_011514611.1:p.Leu307Ser
XM_011516310.1:c.920T>C XP_011514612.1:p.Leu307Ser
XM_011516311.1:c.920T>C XP_011514613.1:p.Leu307Ser
XM_011516312.1:c.920T>C XP_011514614.1:p.Leu307Ser
XM_011516313.1:c.920T>C XP_011514615.1:p.Leu307Ser
XM_011516314.1:c.941T>C XP_011514616.1:p.Leu314Ser
XM_011516315.1:c.260T>C XP_011514617.1:p.Leu87Ser
XR_927478.1:n.1016T>C
XM_011516308.3:c.1190T>C XP_011514610.3:p.Leu397Ser
XM_011516309.3:c.1190T>C XP_011514611.3:p.Leu397Ser
XM_011516310.3:c.1190T>C XP_011514612.3:p.Leu397Ser
XM_011516311.3:c.1190T>C XP_011514613.3:p.Leu397Ser
XM_011516312.3:c.1190T>C XP_011514614.3:p.Leu397Ser
XM_011516313.3:c.1190T>C XP_011514615.2:p.Leu397Ser
XM_011516315.3:c.260T>C XP_011514617.2:p.Leu87Ser
XM_017012323.2:c.920T>C XP_016867812.1:p.Leu307Ser
XR_001744809.2:n.1691T>C
XR_001744810.2:n.1686T>C
NM_000443.4:c.920T>C MANE Select NP_000434.1:p.Leu307Ser
NM_018849.3:c.920T>C NP_061337.1:p.Leu307Ser
NM_018850.3:c.920T>C NP_061338.1:p.Leu307Ser