Canonical Allele Identifier: CA368056777
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402201A>C , CM000669.2:g.87402201A>C GRCh38
NC_000007.13:g.87031517A>C , CM000669.1:g.87031517A>C GRCh37
NC_000007.12:g.86869453A>C NCBI36
NG_007118.1:g.83232T>G
NG_007118.2:g.83232T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3735T>G ENSP00000352135.3:p.Phe1245Leu
ENST00000649586.2:c.3735T>G MANE Select ENSP00000496956.2:p.Phe1245Leu
ENST00000265723.8:c.3756T>G ENSP00000265723.4:p.Phe1252Leu
ENST00000358400.7:c.3594T>G ENSP00000351172.3:p.Phe1198Leu
ENST00000359206.7:c.3735T>G ENSP00000352135.3:p.Phe1245Leu
ENST00000440025.1:c.169T>G
ENST00000453593.5:c.3594T>G ENSP00000392983.1:p.Phe1198Leu
ENST00000467983.1:n.347T>G
NM_000443.3:c.3735T>G NP_000434.1:p.Phe1245Leu
NM_018849.2:c.3756T>G NP_061337.1:p.Phe1252Leu
NM_018850.2:c.3594T>G NP_061338.1:p.Phe1198Leu
XM_011516308.1:c.3756T>G XP_011514610.1:p.Phe1252Leu
XM_011516309.1:c.3735T>G XP_011514611.1:p.Phe1245Leu
XM_011516310.1:c.3651T>G XP_011514612.1:p.Phe1217Leu
XM_011516311.1:c.3627T>G XP_011514613.1:p.Phe1209Leu
XM_011516312.1:c.3615T>G XP_011514614.1:p.Phe1205Leu
XM_011516313.1:c.3594T>G XP_011514615.1:p.Phe1198Leu
XM_011516314.1:c.3777T>G XP_011514616.1:p.Phe1259Leu
XM_011516315.1:c.3096T>G XP_011514617.1:p.Phe1032Leu
XM_011516308.3:c.4026T>G XP_011514610.3:p.Phe1342Leu
XM_011516309.3:c.4005T>G XP_011514611.3:p.Phe1335Leu
XM_011516310.3:c.3921T>G XP_011514612.3:p.Phe1307Leu
XM_011516311.3:c.3897T>G XP_011514613.3:p.Phe1299Leu
XM_011516312.3:c.3885T>G XP_011514614.3:p.Phe1295Leu
XM_011516313.3:c.3864T>G XP_011514615.2:p.Phe1288Leu
XM_011516315.3:c.3096T>G XP_011514617.2:p.Phe1032Leu
XM_017012323.2:c.3756T>G XP_016867812.1:p.Phe1252Leu
XR_001744809.2:n.4264T>G
NM_000443.4:c.3735T>G MANE Select NP_000434.1:p.Phe1245Leu
NM_018849.3:c.3756T>G NP_061337.1:p.Phe1252Leu
NM_018850.3:c.3594T>G NP_061338.1:p.Phe1198Leu