Canonical Allele Identifier: CA368031199
Gene: ABCB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87424043C>A , CM000669.2:g.87424043C>A GRCh38
NC_000007.13:g.87053359C>A , CM000669.1:g.87053359C>A GRCh37
NC_000007.12:g.86891295C>A NCBI36
NG_007118.1:g.61390G>T
NG_007118.2:g.61390G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.2074G>T ENSP00000352135.3:p.Val692Leu
ENST00000643670.1:c.2090G>T ENSP00000496629.1:n.2090G>T
ENST00000649586.2:c.2074G>T MANE Select ENSP00000496956.2:p.Val692Leu
ENST00000265723.8:c.2074G>T ENSP00000265723.4:p.Val692Leu
ENST00000358400.7:c.2074G>T ENSP00000351172.3:p.Val692Leu
ENST00000359206.7:c.2074G>T ENSP00000352135.3:p.Val692Leu
ENST00000453593.5:c.2074G>T ENSP00000392983.1:p.Val692Leu
ENST00000469770.1:n.278G>T
NM_000443.3:c.2074G>T NP_000434.1:p.Val692Leu
NM_018849.2:c.2074G>T NP_061337.1:p.Val692Leu
NM_018850.2:c.2074G>T NP_061338.1:p.Val692Leu
XM_011516308.1:c.2074G>T XP_011514610.1:p.Val692Leu
XM_011516309.1:c.2074G>T XP_011514611.1:p.Val692Leu
XM_011516310.1:c.2074G>T XP_011514612.1:p.Val692Leu
XM_011516311.1:c.2074G>T XP_011514613.1:p.Val692Leu
XM_011516312.1:c.2074G>T XP_011514614.1:p.Val692Leu
XM_011516313.1:c.2074G>T XP_011514615.1:p.Val692Leu
XM_011516314.1:c.2095G>T XP_011514616.1:p.Val699Leu
XM_011516315.1:c.1414G>T XP_011514617.1:p.Val472Leu
XR_927478.1:n.2170G>T
XM_011516308.3:c.2344G>T XP_011514610.3:p.Val782Leu
XM_011516309.3:c.2344G>T XP_011514611.3:p.Val782Leu
XM_011516310.3:c.2344G>T XP_011514612.3:p.Val782Leu
XM_011516311.3:c.2344G>T XP_011514613.3:p.Val782Leu
XM_011516312.3:c.2344G>T XP_011514614.3:p.Val782Leu
XM_011516313.3:c.2344G>T XP_011514615.2:p.Val782Leu
XM_011516315.3:c.1414G>T XP_011514617.2:p.Val472Leu
XM_017012323.2:c.2074G>T XP_016867812.1:p.Val692Leu
XR_001744809.2:n.2845G>T
XR_001744810.2:n.2840G>T
NM_000443.4:c.2074G>T MANE Select NP_000434.1:p.Val692Leu
NM_018849.3:c.2074G>T NP_061337.1:p.Val692Leu
NM_018850.3:c.2074G>T NP_061338.1:p.Val692Leu