Canonical Allele Identifier: CA130625

Gene: ABCB4

Linked Data

• ClinVar Variation Id: 39841
• ClinVar RCV Id: RCV000033068 ; RCV003556101
• dbSNP Id: rs397514620
• MyVariant Identifiers: chr7:g.87069081G>C (hg19) ; chr7:g.87439765G>C (hg38)
• PubMed: PMID:18482588

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87439765G>C , CM000669.2:g.87439765G>C	GRCh38
NC_000007.13:g.87069081G>C , CM000669.1:g.87069081G>C	GRCh37
NC_000007.12:g.86907017G>C	NCBI36
NG_007118.1:g.45668C>G
NG_007118.2:g.45668C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.1633C>G	ENSP00000352135.3:p.Arg545Gly
ENST00000643670.1:c.1649C>G	ENSP00000496629.1:n.1649C>G
ENST00000644106.1:c.*1170C>G	ENSP00000493477.1:n.*1170C>G
ENST00000649586.2:c.1633C>G MANE Select	ENSP00000496956.2:p.Arg545Gly
ENST00000265723.8:c.1633C>G	ENSP00000265723.4:p.Arg545Gly
ENST00000358400.7:c.1633C>G	ENSP00000351172.3:p.Arg545Gly
ENST00000359206.7:c.1633C>G	ENSP00000352135.3:p.Arg545Gly
ENST00000453593.5:c.1633C>G	ENSP00000392983.1:p.Arg545Gly
NM_000443.3:c.1633C>G	NP_000434.1:p.Arg545Gly
NM_018849.2:c.1633C>G	NP_061337.1:p.Arg545Gly
NM_018850.2:c.1633C>G	NP_061338.1:p.Arg545Gly
XM_011516308.1:c.1633C>G	XP_011514610.1:p.Arg545Gly
XM_011516309.1:c.1633C>G	XP_011514611.1:p.Arg545Gly
XM_011516310.1:c.1633C>G	XP_011514612.1:p.Arg545Gly
XM_011516311.1:c.1633C>G	XP_011514613.1:p.Arg545Gly
XM_011516312.1:c.1633C>G	XP_011514614.1:p.Arg545Gly
XM_011516313.1:c.1633C>G	XP_011514615.1:p.Arg545Gly
XM_011516314.1:c.1654C>G	XP_011514616.1:p.Arg552Gly
XM_011516315.1:c.973C>G	XP_011514617.1:p.Arg325Gly
XR_927478.1:n.1729C>G
XM_011516308.3:c.1903C>G	XP_011514610.3:p.Arg635Gly
XM_011516309.3:c.1903C>G	XP_011514611.3:p.Arg635Gly
XM_011516310.3:c.1903C>G	XP_011514612.3:p.Arg635Gly
XM_011516311.3:c.1903C>G	XP_011514613.3:p.Arg635Gly
XM_011516312.3:c.1903C>G	XP_011514614.3:p.Arg635Gly
XM_011516313.3:c.1903C>G	XP_011514615.2:p.Arg635Gly
XM_011516315.3:c.973C>G	XP_011514617.2:p.Arg325Gly
XM_017012323.2:c.1633C>G	XP_016867812.1:p.Arg545Gly
XR_001744809.2:n.2404C>G
XR_001744810.2:n.2399C>G
NM_000443.4:c.1633C>G MANE Select	NP_000434.1:p.Arg545Gly
NM_018849.3:c.1633C>G	NP_061337.1:p.Arg545Gly
NM_018850.3:c.1633C>G	NP_061338.1:p.Arg545Gly