Canonical Allele Identifier: CA368060740

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87041342C>T (hg19) ; chr7:g.87412026C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87412026C>T , CM000669.2:g.87412026C>T	GRCh38
NC_000007.13:g.87041342C>T , CM000669.1:g.87041342C>T	GRCh37
NC_000007.12:g.86879278C>T	NCBI36
NG_007118.1:g.73407G>A
NG_007118.2:g.73407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.2791G>A	ENSP00000352135.3:p.Val931Met
ENST00000649586.2:c.2791G>A MANE Select	ENSP00000496956.2:p.Val931Met
ENST00000265723.8:c.2791G>A	ENSP00000265723.4:p.Val931Met
ENST00000358400.7:c.2783+1591G>A	ENSP00000351172.3:n.2783+1591G>A
ENST00000359206.7:c.2791G>A	ENSP00000352135.3:p.Val931Met
ENST00000453593.5:c.2783+1591G>A	ENSP00000392983.1:n.2783+1591G>A
NM_000443.3:c.2791G>A	NP_000434.1:p.Val931Met
NM_018849.2:c.2791G>A	NP_061337.1:p.Val931Met
NM_018850.2:c.2783+1591G>A	NP_061338.1:n.2783+1591G>A
XM_011516308.1:c.2791G>A	XP_011514610.1:p.Val931Met
XM_011516309.1:c.2791G>A	XP_011514611.1:p.Val931Met
XM_011516310.1:c.2686G>A	XP_011514612.1:p.Val896Met
XM_011516311.1:c.2784-122G>A	XP_011514613.1:n.2784-122G>A
XM_011516312.1:c.2783+1591G>A	XP_011514614.1:n.2783+1591G>A
XM_011516313.1:c.2783+1591G>A	XP_011514615.1:n.2783+1591G>A
XM_011516314.1:c.2812G>A	XP_011514616.1:p.Val938Met
XM_011516315.1:c.2131G>A	XP_011514617.1:p.Val711Met
XR_927478.1:n.2779-2634G>A
XM_011516308.3:c.3061G>A	XP_011514610.3:p.Val1021Met
XM_011516309.3:c.3061G>A	XP_011514611.3:p.Val1021Met
XM_011516310.3:c.2956G>A	XP_011514612.3:p.Val986Met
XM_011516311.3:c.3054-122G>A	XP_011514613.3:n.3054-122G>A
XM_011516312.3:c.3053+1591G>A	XP_011514614.3:n.3053+1591G>A
XM_011516313.3:c.3053+1591G>A	XP_011514615.2:n.3053+1591G>A
XM_011516315.3:c.2131G>A	XP_011514617.2:p.Val711Met
XM_017012323.2:c.2791G>A	XP_016867812.1:p.Val931Met
XR_001744809.2:n.3454-2634G>A
NM_000443.4:c.2791G>A MANE Select	NP_000434.1:p.Val931Met
NM_018849.3:c.2791G>A	NP_061337.1:p.Val931Met
NM_018850.3:c.2783+1591G>A	NP_061338.1:n.2783+1591G>A