Canonical Allele Identifier: CA368061239

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87046692A>T (hg19) ; chr7:g.87417376A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87417376A>T , CM000669.2:g.87417376A>T	GRCh38
NC_000007.13:g.87046692A>T , CM000669.1:g.87046692A>T	GRCh37
NC_000007.12:g.86884628A>T	NCBI36
NG_007118.1:g.68057T>A
NG_007118.2:g.68057T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.2618T>A	ENSP00000352135.3:p.Val873Asp
ENST00000649586.2:c.2618T>A MANE Select	ENSP00000496956.2:p.Val873Asp
ENST00000265723.8:c.2618T>A	ENSP00000265723.4:p.Val873Asp
ENST00000358400.7:c.2618T>A	ENSP00000351172.3:p.Val873Asp
ENST00000359206.7:c.2618T>A	ENSP00000352135.3:p.Val873Asp
ENST00000453593.5:c.2618T>A	ENSP00000392983.1:p.Val873Asp
NM_000443.3:c.2618T>A	NP_000434.1:p.Val873Asp
NM_018849.2:c.2618T>A	NP_061337.1:p.Val873Asp
NM_018850.2:c.2618T>A	NP_061338.1:p.Val873Asp
XM_011516308.1:c.2618T>A	XP_011514610.1:p.Val873Asp
XM_011516309.1:c.2618T>A	XP_011514611.1:p.Val873Asp
XM_011516310.1:c.2513T>A	XP_011514612.1:p.Val838Asp
XM_011516311.1:c.2618T>A	XP_011514613.1:p.Val873Asp
XM_011516312.1:c.2618T>A	XP_011514614.1:p.Val873Asp
XM_011516313.1:c.2618T>A	XP_011514615.1:p.Val873Asp
XM_011516314.1:c.2639T>A	XP_011514616.1:p.Val880Asp
XM_011516315.1:c.1958T>A	XP_011514617.1:p.Val653Asp
XR_927478.1:n.2714T>A
XM_011516308.3:c.2888T>A	XP_011514610.3:p.Val963Asp
XM_011516309.3:c.2888T>A	XP_011514611.3:p.Val963Asp
XM_011516310.3:c.2783T>A	XP_011514612.3:p.Val928Asp
XM_011516311.3:c.2888T>A	XP_011514613.3:p.Val963Asp
XM_011516312.3:c.2888T>A	XP_011514614.3:p.Val963Asp
XM_011516313.3:c.2888T>A	XP_011514615.2:p.Val963Asp
XM_011516315.3:c.1958T>A	XP_011514617.2:p.Val653Asp
XM_017012323.2:c.2618T>A	XP_016867812.1:p.Val873Asp
XR_001744809.2:n.3389T>A
NM_000443.4:c.2618T>A MANE Select	NP_000434.1:p.Val873Asp
NM_018849.3:c.2618T>A	NP_061337.1:p.Val873Asp
NM_018850.3:c.2618T>A	NP_061338.1:p.Val873Asp