Canonical Allele Identifier: CA1723573389

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87412083C= , CM000669.2:g.87412083C=	GRCh38
NC_000007.13:g.87041399C= , CM000669.1:g.87041399C=	GRCh37
NC_000007.12:g.86879335C=	NCBI36
NG_007118.1:g.73350G=
NG_007118.2:g.73350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2784-50G=	ENSP00000352135.3:n.2784-50G=
ENST00000649586.2:c.2784-50G= MANE Select	ENSP00000496956.2:n.2784-50G=
ENST00000265723.8:c.2784-50G=	ENSP00000265723.4:n.2784-50G=
ENST00000358400.7:c.2783+1534G=	ENSP00000351172.3:n.2783+1534G=
ENST00000359206.7:c.2784-50G=	ENSP00000352135.3:n.2784-50G=
ENST00000453593.5:c.2783+1534G=	ENSP00000392983.1:n.2783+1534G=
NM_000443.3:c.2784-50G=	NP_000434.1:n.2784-50G=
NM_018849.2:c.2784-50G=	NP_061337.1:n.2784-50G=
NM_018850.2:c.2783+1534G=	NP_061338.1:n.2783+1534G=
XM_011516308.1:c.2784-50G=	XP_011514610.1:n.2784-50G=
XM_011516309.1:c.2784-50G=	XP_011514611.1:n.2784-50G=
XM_011516310.1:c.2679-50G=	XP_011514612.1:n.2679-50G=
XM_011516311.1:c.2784-179G=	XP_011514613.1:n.2784-179G=
XM_011516312.1:c.2783+1534G=	XP_011514614.1:n.2783+1534G=
XM_011516313.1:c.2783+1534G=	XP_011514615.1:n.2783+1534G=
XM_011516314.1:c.2805-50G=	XP_011514616.1:n.2805-50G=
XM_011516315.1:c.2124-50G=	XP_011514617.1:n.2124-50G=
XR_927478.1:n.2779-2691G=
XM_011516308.3:c.3054-50G=	XP_011514610.3:n.3054-50G=
XM_011516309.3:c.3054-50G=	XP_011514611.3:n.3054-50G=
XM_011516310.3:c.2949-50G=	XP_011514612.3:n.2949-50G=
XM_011516311.3:c.3054-179G=	XP_011514613.3:n.3054-179G=
XM_011516312.3:c.3053+1534G=	XP_011514614.3:n.3053+1534G=
XM_011516313.3:c.3053+1534G=	XP_011514615.2:n.3053+1534G=
XM_011516315.3:c.2124-50G=	XP_011514617.2:n.2124-50G=
XM_017012323.2:c.2784-50G=	XP_016867812.1:n.2784-50G=
XR_001744809.2:n.3454-2691G=
NM_000443.4:c.2784-50G= MANE Select	NP_000434.1:n.2784-50G=
NM_018849.3:c.2784-50G=	NP_061337.1:n.2784-50G=
NM_018850.3:c.2783+1534G=	NP_061338.1:n.2783+1534G=