Canonical Allele Identifier: CA456357887

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87041286A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87411970A>G , CM000669.2:g.87411970A>G	GRCh38
NC_000007.13:g.87041286A>G , CM000669.1:g.87041286A>G	GRCh37
NC_000007.12:g.86879222A>G	NCBI36
NG_007118.1:g.73463T>C
NG_007118.2:g.73463T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2847T>C	ENSP00000352135.3:p.Tyr949=
ENST00000649586.2:c.2847T>C MANE Select	ENSP00000496956.2:p.Tyr949=
ENST00000265723.8:c.2847T>C	ENSP00000265723.4:p.Tyr949=
ENST00000358400.7:c.2783+1647T>C	ENSP00000351172.3:n.2783+1647T>C
ENST00000359206.7:c.2847T>C	ENSP00000352135.3:p.Tyr949=
ENST00000453593.5:c.2783+1647T>C	ENSP00000392983.1:n.2783+1647T>C
NM_000443.3:c.2847T>C	NP_000434.1:p.Tyr949=
NM_018849.2:c.2847T>C	NP_061337.1:p.Tyr949=
NM_018850.2:c.2783+1647T>C	NP_061338.1:n.2783+1647T>C
XM_011516308.1:c.2847T>C	XP_011514610.1:p.Tyr949=
XM_011516309.1:c.2847T>C	XP_011514611.1:p.Tyr949=
XM_011516310.1:c.2742T>C	XP_011514612.1:p.Tyr914=
XM_011516311.1:c.2784-66T>C	XP_011514613.1:n.2784-66T>C
XM_011516312.1:c.2783+1647T>C	XP_011514614.1:n.2783+1647T>C
XM_011516313.1:c.2783+1647T>C	XP_011514615.1:n.2783+1647T>C
XM_011516314.1:c.2868T>C	XP_011514616.1:p.Tyr956=
XM_011516315.1:c.2187T>C	XP_011514617.1:p.Tyr729=
XR_927478.1:n.2779-2578T>C
XM_011516308.3:c.3117T>C	XP_011514610.3:p.Tyr1039=
XM_011516309.3:c.3117T>C	XP_011514611.3:p.Tyr1039=
XM_011516310.3:c.3012T>C	XP_011514612.3:p.Tyr1004=
XM_011516311.3:c.3054-66T>C	XP_011514613.3:n.3054-66T>C
XM_011516312.3:c.3053+1647T>C	XP_011514614.3:n.3053+1647T>C
XM_011516313.3:c.3053+1647T>C	XP_011514615.2:n.3053+1647T>C
XM_011516315.3:c.2187T>C	XP_011514617.2:p.Tyr729=
XM_017012323.2:c.2847T>C	XP_016867812.1:p.Tyr949=
XR_001744809.2:n.3454-2578T>C
NM_000443.4:c.2847T>C MANE Select	NP_000434.1:p.Tyr949=
NM_018849.3:c.2847T>C	NP_061337.1:p.Tyr949=
NM_018850.3:c.2783+1647T>C	NP_061338.1:n.2783+1647T>C