Canonical Allele Identifier: CA456356311

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031580G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402264G>C , CM000669.2:g.87402264G>C	GRCh38
NC_000007.13:g.87031580G>C , CM000669.1:g.87031580G>C	GRCh37
NC_000007.12:g.86869516G>C	NCBI36
NG_007118.1:g.83169C>G
NG_007118.2:g.83169C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3672C>G	ENSP00000352135.3:p.Arg1224=
ENST00000649586.2:c.3672C>G MANE Select	ENSP00000496956.2:p.Arg1224=
ENST00000265723.8:c.3693C>G	ENSP00000265723.4:p.Arg1231=
ENST00000358400.7:c.3531C>G	ENSP00000351172.3:p.Arg1177=
ENST00000359206.7:c.3672C>G	ENSP00000352135.3:p.Arg1224=
ENST00000440025.1:c.106C>G
ENST00000453593.5:c.3531C>G	ENSP00000392983.1:p.Arg1177=
ENST00000467983.1:n.284C>G
NM_000443.3:c.3672C>G	NP_000434.1:p.Arg1224=
NM_018849.2:c.3693C>G	NP_061337.1:p.Arg1231=
NM_018850.2:c.3531C>G	NP_061338.1:p.Arg1177=
XM_011516308.1:c.3693C>G	XP_011514610.1:p.Arg1231=
XM_011516309.1:c.3672C>G	XP_011514611.1:p.Arg1224=
XM_011516310.1:c.3588C>G	XP_011514612.1:p.Arg1196=
XM_011516311.1:c.3564C>G	XP_011514613.1:p.Arg1188=
XM_011516312.1:c.3552C>G	XP_011514614.1:p.Arg1184=
XM_011516313.1:c.3531C>G	XP_011514615.1:p.Arg1177=
XM_011516314.1:c.3714C>G	XP_011514616.1:p.Arg1238=
XM_011516315.1:c.3033C>G	XP_011514617.1:p.Arg1011=
XM_011516308.3:c.3963C>G	XP_011514610.3:p.Arg1321=
XM_011516309.3:c.3942C>G	XP_011514611.3:p.Arg1314=
XM_011516310.3:c.3858C>G	XP_011514612.3:p.Arg1286=
XM_011516311.3:c.3834C>G	XP_011514613.3:p.Arg1278=
XM_011516312.3:c.3822C>G	XP_011514614.3:p.Arg1274=
XM_011516313.3:c.3801C>G	XP_011514615.2:p.Arg1267=
XM_011516315.3:c.3033C>G	XP_011514617.2:p.Arg1011=
XM_017012323.2:c.3693C>G	XP_016867812.1:p.Arg1231=
XR_001744809.2:n.4201C>G
NM_000443.4:c.3672C>G MANE Select	NP_000434.1:p.Arg1224=
NM_018849.3:c.3693C>G	NP_061337.1:p.Arg1231=
NM_018850.3:c.3531C>G	NP_061338.1:p.Arg1177=