Canonical Allele Identifier: CA456348122

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87053255C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87423939C>G , CM000669.2:g.87423939C>G	GRCh38
NC_000007.13:g.87053255C>G , CM000669.1:g.87053255C>G	GRCh37
NC_000007.12:g.86891191C>G	NCBI36
NG_007118.1:g.61494G>C
NG_007118.2:g.61494G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2178G>C	ENSP00000352135.3:p.Pro726=
ENST00000643670.1:c.2194G>C	ENSP00000496629.1:n.2194G>C
ENST00000649586.2:c.2178G>C MANE Select	ENSP00000496956.2:p.Pro726=
ENST00000265723.8:c.2178G>C	ENSP00000265723.4:p.Pro726=
ENST00000358400.7:c.2178G>C	ENSP00000351172.3:p.Pro726=
ENST00000359206.7:c.2178G>C	ENSP00000352135.3:p.Pro726=
ENST00000453593.5:c.2178G>C	ENSP00000392983.1:p.Pro726=
ENST00000469770.1:n.382G>C
NM_000443.3:c.2178G>C	NP_000434.1:p.Pro726=
NM_018849.2:c.2178G>C	NP_061337.1:p.Pro726=
NM_018850.2:c.2178G>C	NP_061338.1:p.Pro726=
XM_011516308.1:c.2178G>C	XP_011514610.1:p.Pro726=
XM_011516309.1:c.2178G>C	XP_011514611.1:p.Pro726=
XM_011516310.1:c.2178G>C	XP_011514612.1:p.Pro726=
XM_011516311.1:c.2178G>C	XP_011514613.1:p.Pro726=
XM_011516312.1:c.2178G>C	XP_011514614.1:p.Pro726=
XM_011516313.1:c.2178G>C	XP_011514615.1:p.Pro726=
XM_011516314.1:c.2199G>C	XP_011514616.1:p.Pro733=
XM_011516315.1:c.1518G>C	XP_011514617.1:p.Pro506=
XR_927478.1:n.2274G>C
XM_011516308.3:c.2448G>C	XP_011514610.3:p.Pro816=
XM_011516309.3:c.2448G>C	XP_011514611.3:p.Pro816=
XM_011516310.3:c.2448G>C	XP_011514612.3:p.Pro816=
XM_011516311.3:c.2448G>C	XP_011514613.3:p.Pro816=
XM_011516312.3:c.2448G>C	XP_011514614.3:p.Pro816=
XM_011516313.3:c.2448G>C	XP_011514615.2:p.Pro816=
XM_011516315.3:c.1518G>C	XP_011514617.2:p.Pro506=
XM_017012323.2:c.2178G>C	XP_016867812.1:p.Pro726=
XR_001744809.2:n.2949G>C
XR_001744810.2:n.2944G>C
NM_000443.4:c.2178G>C MANE Select	NP_000434.1:p.Pro726=
NM_018849.3:c.2178G>C	NP_061337.1:p.Pro726=
NM_018850.3:c.2178G>C	NP_061338.1:p.Pro726=