Canonical Allele Identifier: CA368056784
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402203A>G , CM000669.2:g.87402203A>G GRCh38
NC_000007.13:g.87031519A>G , CM000669.1:g.87031519A>G GRCh37
NC_000007.12:g.86869455A>G NCBI36
NG_007118.1:g.83230T>C
NG_007118.2:g.83230T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3733T>C ENSP00000352135.3:p.Phe1245Leu
ENST00000649586.2:c.3733T>C MANE Select ENSP00000496956.2:p.Phe1245Leu
ENST00000265723.8:c.3754T>C ENSP00000265723.4:p.Phe1252Leu
ENST00000358400.7:c.3592T>C ENSP00000351172.3:p.Phe1198Leu
ENST00000359206.7:c.3733T>C ENSP00000352135.3:p.Phe1245Leu
ENST00000440025.1:c.167T>C
ENST00000453593.5:c.3592T>C ENSP00000392983.1:p.Phe1198Leu
ENST00000467983.1:n.345T>C
NM_000443.3:c.3733T>C NP_000434.1:p.Phe1245Leu
NM_018849.2:c.3754T>C NP_061337.1:p.Phe1252Leu
NM_018850.2:c.3592T>C NP_061338.1:p.Phe1198Leu
XM_011516308.1:c.3754T>C XP_011514610.1:p.Phe1252Leu
XM_011516309.1:c.3733T>C XP_011514611.1:p.Phe1245Leu
XM_011516310.1:c.3649T>C XP_011514612.1:p.Phe1217Leu
XM_011516311.1:c.3625T>C XP_011514613.1:p.Phe1209Leu
XM_011516312.1:c.3613T>C XP_011514614.1:p.Phe1205Leu
XM_011516313.1:c.3592T>C XP_011514615.1:p.Phe1198Leu
XM_011516314.1:c.3775T>C XP_011514616.1:p.Phe1259Leu
XM_011516315.1:c.3094T>C XP_011514617.1:p.Phe1032Leu
XM_011516308.3:c.4024T>C XP_011514610.3:p.Phe1342Leu
XM_011516309.3:c.4003T>C XP_011514611.3:p.Phe1335Leu
XM_011516310.3:c.3919T>C XP_011514612.3:p.Phe1307Leu
XM_011516311.3:c.3895T>C XP_011514613.3:p.Phe1299Leu
XM_011516312.3:c.3883T>C XP_011514614.3:p.Phe1295Leu
XM_011516313.3:c.3862T>C XP_011514615.2:p.Phe1288Leu
XM_011516315.3:c.3094T>C XP_011514617.2:p.Phe1032Leu
XM_017012323.2:c.3754T>C XP_016867812.1:p.Phe1252Leu
XR_001744809.2:n.4262T>C
NM_000443.4:c.3733T>C MANE Select NP_000434.1:p.Phe1245Leu
NM_018849.3:c.3754T>C NP_061337.1:p.Phe1252Leu
NM_018850.3:c.3592T>C NP_061338.1:p.Phe1198Leu