Canonical Allele Identifier: CA456356312

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031583G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402267G>A , CM000669.2:g.87402267G>A	GRCh38
NC_000007.13:g.87031583G>A , CM000669.1:g.87031583G>A	GRCh37
NC_000007.12:g.86869519G>A	NCBI36
NG_007118.1:g.83166C>T
NG_007118.2:g.83166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3669C>T	ENSP00000352135.3:p.Gly1223=
ENST00000649586.2:c.3669C>T MANE Select	ENSP00000496956.2:p.Gly1223=
ENST00000265723.8:c.3690C>T	ENSP00000265723.4:p.Gly1230=
ENST00000358400.7:c.3528C>T	ENSP00000351172.3:p.Gly1176=
ENST00000359206.7:c.3669C>T	ENSP00000352135.3:p.Gly1223=
ENST00000440025.1:c.103C>T
ENST00000453593.5:c.3528C>T	ENSP00000392983.1:p.Gly1176=
ENST00000467983.1:n.281C>T
NM_000443.3:c.3669C>T	NP_000434.1:p.Gly1223=
NM_018849.2:c.3690C>T	NP_061337.1:p.Gly1230=
NM_018850.2:c.3528C>T	NP_061338.1:p.Gly1176=
XM_011516308.1:c.3690C>T	XP_011514610.1:p.Gly1230=
XM_011516309.1:c.3669C>T	XP_011514611.1:p.Gly1223=
XM_011516310.1:c.3585C>T	XP_011514612.1:p.Gly1195=
XM_011516311.1:c.3561C>T	XP_011514613.1:p.Gly1187=
XM_011516312.1:c.3549C>T	XP_011514614.1:p.Gly1183=
XM_011516313.1:c.3528C>T	XP_011514615.1:p.Gly1176=
XM_011516314.1:c.3711C>T	XP_011514616.1:p.Gly1237=
XM_011516315.1:c.3030C>T	XP_011514617.1:p.Gly1010=
XM_011516308.3:c.3960C>T	XP_011514610.3:p.Gly1320=
XM_011516309.3:c.3939C>T	XP_011514611.3:p.Gly1313=
XM_011516310.3:c.3855C>T	XP_011514612.3:p.Gly1285=
XM_011516311.3:c.3831C>T	XP_011514613.3:p.Gly1277=
XM_011516312.3:c.3819C>T	XP_011514614.3:p.Gly1273=
XM_011516313.3:c.3798C>T	XP_011514615.2:p.Gly1266=
XM_011516315.3:c.3030C>T	XP_011514617.2:p.Gly1010=
XM_017012323.2:c.3690C>T	XP_016867812.1:p.Gly1230=
XR_001744809.2:n.4198C>T
NM_000443.4:c.3669C>T MANE Select	NP_000434.1:p.Gly1223=
NM_018849.3:c.3690C>T	NP_061337.1:p.Gly1230=
NM_018850.3:c.3528C>T	NP_061338.1:p.Gly1176=