Canonical Allele Identifier: CA456351038

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87076458A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87447142A>T , CM000669.2:g.87447142A>T	GRCh38
NC_000007.13:g.87076458A>T , CM000669.1:g.87076458A>T	GRCh37
NC_000007.12:g.86914394A>T	NCBI36
NG_007118.1:g.38291T>A
NG_007118.2:g.38291T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.897T>A	ENSP00000352135.3:p.Ile299=
ENST00000643670.1:c.913T>A	ENSP00000496629.1:n.913T>A
ENST00000644106.1:c.*434T>A	ENSP00000493477.1:n.*434T>A
ENST00000649586.2:c.897T>A MANE Select	ENSP00000496956.2:p.Ile299=
ENST00000265723.8:c.897T>A	ENSP00000265723.4:p.Ile299=
ENST00000358400.7:c.897T>A	ENSP00000351172.3:p.Ile299=
ENST00000359206.7:c.897T>A	ENSP00000352135.3:p.Ile299=
ENST00000453593.5:c.897T>A	ENSP00000392983.1:p.Ile299=
NM_000443.3:c.897T>A	NP_000434.1:p.Ile299=
NM_018849.2:c.897T>A	NP_061337.1:p.Ile299=
NM_018850.2:c.897T>A	NP_061338.1:p.Ile299=
XM_011516308.1:c.897T>A	XP_011514610.1:p.Ile299=
XM_011516309.1:c.897T>A	XP_011514611.1:p.Ile299=
XM_011516310.1:c.897T>A	XP_011514612.1:p.Ile299=
XM_011516311.1:c.897T>A	XP_011514613.1:p.Ile299=
XM_011516312.1:c.897T>A	XP_011514614.1:p.Ile299=
XM_011516313.1:c.897T>A	XP_011514615.1:p.Ile299=
XM_011516314.1:c.918T>A	XP_011514616.1:p.Ile306=
XM_011516315.1:c.237T>A	XP_011514617.1:p.Ile79=
XR_927478.1:n.993T>A
XM_011516308.3:c.1167T>A	XP_011514610.3:p.Ile389=
XM_011516309.3:c.1167T>A	XP_011514611.3:p.Ile389=
XM_011516310.3:c.1167T>A	XP_011514612.3:p.Ile389=
XM_011516311.3:c.1167T>A	XP_011514613.3:p.Ile389=
XM_011516312.3:c.1167T>A	XP_011514614.3:p.Ile389=
XM_011516313.3:c.1167T>A	XP_011514615.2:p.Ile389=
XM_011516315.3:c.237T>A	XP_011514617.2:p.Ile79=
XM_017012323.2:c.897T>A	XP_016867812.1:p.Ile299=
XR_001744809.2:n.1668T>A
XR_001744810.2:n.1663T>A
NM_000443.4:c.897T>A MANE Select	NP_000434.1:p.Ile299=
NM_018849.3:c.897T>A	NP_061337.1:p.Ile299=
NM_018850.3:c.897T>A	NP_061338.1:p.Ile299=