Canonical Allele Identifier: CA368035327

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87060842G>C (hg19) ; chr7:g.87431526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87431526G>C , CM000669.2:g.87431526G>C	GRCh38
NC_000007.13:g.87060842G>C , CM000669.1:g.87060842G>C	GRCh37
NC_000007.12:g.86898778G>C	NCBI36
NG_007118.1:g.53907C>G
NG_007118.2:g.53907C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.1771C>G	ENSP00000352135.3:p.Leu591Val
ENST00000643670.1:c.1787C>G	ENSP00000496629.1:n.1787C>G
ENST00000644106.1:c.*1308C>G	ENSP00000493477.1:n.*1308C>G
ENST00000649586.2:c.1771C>G MANE Select	ENSP00000496956.2:p.Leu591Val
ENST00000265723.8:c.1771C>G	ENSP00000265723.4:p.Leu591Val
ENST00000358400.7:c.1771C>G	ENSP00000351172.3:p.Leu591Val
ENST00000359206.7:c.1771C>G	ENSP00000352135.3:p.Leu591Val
ENST00000453593.5:c.1771C>G	ENSP00000392983.1:p.Leu591Val
NM_000443.3:c.1771C>G	NP_000434.1:p.Leu591Val
NM_018849.2:c.1771C>G	NP_061337.1:p.Leu591Val
NM_018850.2:c.1771C>G	NP_061338.1:p.Leu591Val
XM_011516308.1:c.1771C>G	XP_011514610.1:p.Leu591Val
XM_011516309.1:c.1771C>G	XP_011514611.1:p.Leu591Val
XM_011516310.1:c.1771C>G	XP_011514612.1:p.Leu591Val
XM_011516311.1:c.1771C>G	XP_011514613.1:p.Leu591Val
XM_011516312.1:c.1771C>G	XP_011514614.1:p.Leu591Val
XM_011516313.1:c.1771C>G	XP_011514615.1:p.Leu591Val
XM_011516314.1:c.1792C>G	XP_011514616.1:p.Leu598Val
XM_011516315.1:c.1111C>G	XP_011514617.1:p.Leu371Val
XR_927478.1:n.1867C>G
XM_011516308.3:c.2041C>G	XP_011514610.3:p.Leu681Val
XM_011516309.3:c.2041C>G	XP_011514611.3:p.Leu681Val
XM_011516310.3:c.2041C>G	XP_011514612.3:p.Leu681Val
XM_011516311.3:c.2041C>G	XP_011514613.3:p.Leu681Val
XM_011516312.3:c.2041C>G	XP_011514614.3:p.Leu681Val
XM_011516313.3:c.2041C>G	XP_011514615.2:p.Leu681Val
XM_011516315.3:c.1111C>G	XP_011514617.2:p.Leu371Val
XM_017012323.2:c.1771C>G	XP_016867812.1:p.Leu591Val
XR_001744809.2:n.2542C>G
XR_001744810.2:n.2537C>G
NM_000443.4:c.1771C>G MANE Select	NP_000434.1:p.Leu591Val
NM_018849.3:c.1771C>G	NP_061337.1:p.Leu591Val
NM_018850.3:c.1771C>G	NP_061338.1:p.Leu591Val