Canonical Allele Identifier: CA368060578

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87041269C>T (hg19) ; chr7:g.87411953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87411953C>T , CM000669.2:g.87411953C>T	GRCh38
NC_000007.13:g.87041269C>T , CM000669.1:g.87041269C>T	GRCh37
NC_000007.12:g.86879205C>T	NCBI36
NG_007118.1:g.73480G>A
NG_007118.2:g.73480G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.2864G>A	ENSP00000352135.3:p.Cys955Tyr
ENST00000649586.2:c.2864G>A MANE Select	ENSP00000496956.2:p.Cys955Tyr
ENST00000265723.8:c.2864G>A	ENSP00000265723.4:p.Cys955Tyr
ENST00000358400.7:c.2783+1664G>A	ENSP00000351172.3:n.2783+1664G>A
ENST00000359206.7:c.2864G>A	ENSP00000352135.3:p.Cys955Tyr
ENST00000453593.5:c.2783+1664G>A	ENSP00000392983.1:n.2783+1664G>A
NM_000443.3:c.2864G>A	NP_000434.1:p.Cys955Tyr
NM_018849.2:c.2864G>A	NP_061337.1:p.Cys955Tyr
NM_018850.2:c.2783+1664G>A	NP_061338.1:n.2783+1664G>A
XM_011516308.1:c.2864G>A	XP_011514610.1:p.Cys955Tyr
XM_011516309.1:c.2864G>A	XP_011514611.1:p.Cys955Tyr
XM_011516310.1:c.2759G>A	XP_011514612.1:p.Cys920Tyr
XM_011516311.1:c.2784-49G>A	XP_011514613.1:n.2784-49G>A
XM_011516312.1:c.2783+1664G>A	XP_011514614.1:n.2783+1664G>A
XM_011516313.1:c.2783+1664G>A	XP_011514615.1:n.2783+1664G>A
XM_011516314.1:c.2885G>A	XP_011514616.1:p.Cys962Tyr
XM_011516315.1:c.2204G>A	XP_011514617.1:p.Cys735Tyr
XR_927478.1:n.2779-2561G>A
XM_011516308.3:c.3134G>A	XP_011514610.3:p.Cys1045Tyr
XM_011516309.3:c.3134G>A	XP_011514611.3:p.Cys1045Tyr
XM_011516310.3:c.3029G>A	XP_011514612.3:p.Cys1010Tyr
XM_011516311.3:c.3054-49G>A	XP_011514613.3:n.3054-49G>A
XM_011516312.3:c.3053+1664G>A	XP_011514614.3:n.3053+1664G>A
XM_011516313.3:c.3053+1664G>A	XP_011514615.2:n.3053+1664G>A
XM_011516315.3:c.2204G>A	XP_011514617.2:p.Cys735Tyr
XM_017012323.2:c.2864G>A	XP_016867812.1:p.Cys955Tyr
XR_001744809.2:n.3454-2561G>A
NM_000443.4:c.2864G>A MANE Select	NP_000434.1:p.Cys955Tyr
NM_018849.3:c.2864G>A	NP_061337.1:p.Cys955Tyr
NM_018850.3:c.2783+1664G>A	NP_061338.1:n.2783+1664G>A