Canonical Allele Identifier: CA368056808
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402214A>T , CM000669.2:g.87402214A>T GRCh38
NC_000007.13:g.87031530A>T , CM000669.1:g.87031530A>T GRCh37
NC_000007.12:g.86869466A>T NCBI36
NG_007118.1:g.83219T>A
NG_007118.2:g.83219T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3722T>A ENSP00000352135.3:p.Leu1241Ter
ENST00000649586.2:c.3722T>A MANE Select ENSP00000496956.2:p.Leu1241Ter
ENST00000265723.8:c.3743T>A ENSP00000265723.4:p.Leu1248Ter
ENST00000358400.7:c.3581T>A ENSP00000351172.3:p.Leu1194Ter
ENST00000359206.7:c.3722T>A ENSP00000352135.3:p.Leu1241Ter
ENST00000440025.1:c.156T>A
ENST00000453593.5:c.3581T>A ENSP00000392983.1:p.Leu1194Ter
ENST00000467983.1:n.334T>A
NM_000443.3:c.3722T>A NP_000434.1:p.Leu1241Ter
NM_018849.2:c.3743T>A NP_061337.1:p.Leu1248Ter
NM_018850.2:c.3581T>A NP_061338.1:p.Leu1194Ter
XM_011516308.1:c.3743T>A XP_011514610.1:p.Leu1248Ter
XM_011516309.1:c.3722T>A XP_011514611.1:p.Leu1241Ter
XM_011516310.1:c.3638T>A XP_011514612.1:p.Leu1213Ter
XM_011516311.1:c.3614T>A XP_011514613.1:p.Leu1205Ter
XM_011516312.1:c.3602T>A XP_011514614.1:p.Leu1201Ter
XM_011516313.1:c.3581T>A XP_011514615.1:p.Leu1194Ter
XM_011516314.1:c.3764T>A XP_011514616.1:p.Leu1255Ter
XM_011516315.1:c.3083T>A XP_011514617.1:p.Leu1028Ter
XM_011516308.3:c.4013T>A XP_011514610.3:p.Leu1338Ter
XM_011516309.3:c.3992T>A XP_011514611.3:p.Leu1331Ter
XM_011516310.3:c.3908T>A XP_011514612.3:p.Leu1303Ter
XM_011516311.3:c.3884T>A XP_011514613.3:p.Leu1295Ter
XM_011516312.3:c.3872T>A XP_011514614.3:p.Leu1291Ter
XM_011516313.3:c.3851T>A XP_011514615.2:p.Leu1284Ter
XM_011516315.3:c.3083T>A XP_011514617.2:p.Leu1028Ter
XM_017012323.2:c.3743T>A XP_016867812.1:p.Leu1248Ter
XR_001744809.2:n.4251T>A
NM_000443.4:c.3722T>A MANE Select NP_000434.1:p.Leu1241Ter
NM_018849.3:c.3743T>A NP_061337.1:p.Leu1248Ter
NM_018850.3:c.3581T>A NP_061338.1:p.Leu1194Ter