Canonical Allele Identifier: CA368038109

Gene: ABCB4

Linked Data

• dbSNP Id: rs1329665367
• gnomAD v2: 7-87069009-C-T
• gnomAD v4: 7-87439693-C-T
• MyVariant Identifiers: chr7:g.87069009C>T (hg19) ; chr7:g.87439693C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87439693C>T , CM000669.2:g.87439693C>T	GRCh38
NC_000007.13:g.87069009C>T , CM000669.1:g.87069009C>T	GRCh37
NC_000007.12:g.86906945C>T	NCBI36
NG_007118.1:g.45740G>A
NG_007118.2:g.45740G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.1705G>A	ENSP00000352135.3:p.Ala569Thr
ENST00000643670.1:c.1721G>A	ENSP00000496629.1:n.1721G>A
ENST00000644106.1:c.*1242G>A	ENSP00000493477.1:n.*1242G>A
ENST00000649586.2:c.1705G>A MANE Select	ENSP00000496956.2:p.Ala569Thr
ENST00000265723.8:c.1705G>A	ENSP00000265723.4:p.Ala569Thr
ENST00000358400.7:c.1705G>A	ENSP00000351172.3:p.Ala569Thr
ENST00000359206.7:c.1705G>A	ENSP00000352135.3:p.Ala569Thr
ENST00000453593.5:c.1705G>A	ENSP00000392983.1:p.Ala569Thr
NM_000443.3:c.1705G>A	NP_000434.1:p.Ala569Thr
NM_018849.2:c.1705G>A	NP_061337.1:p.Ala569Thr
NM_018850.2:c.1705G>A	NP_061338.1:p.Ala569Thr
XM_011516308.1:c.1705G>A	XP_011514610.1:p.Ala569Thr
XM_011516309.1:c.1705G>A	XP_011514611.1:p.Ala569Thr
XM_011516310.1:c.1705G>A	XP_011514612.1:p.Ala569Thr
XM_011516311.1:c.1705G>A	XP_011514613.1:p.Ala569Thr
XM_011516312.1:c.1705G>A	XP_011514614.1:p.Ala569Thr
XM_011516313.1:c.1705G>A	XP_011514615.1:p.Ala569Thr
XM_011516314.1:c.1726G>A	XP_011514616.1:p.Ala576Thr
XM_011516315.1:c.1045G>A	XP_011514617.1:p.Ala349Thr
XR_927478.1:n.1801G>A
XM_011516308.3:c.1975G>A	XP_011514610.3:p.Ala659Thr
XM_011516309.3:c.1975G>A	XP_011514611.3:p.Ala659Thr
XM_011516310.3:c.1975G>A	XP_011514612.3:p.Ala659Thr
XM_011516311.3:c.1975G>A	XP_011514613.3:p.Ala659Thr
XM_011516312.3:c.1975G>A	XP_011514614.3:p.Ala659Thr
XM_011516313.3:c.1975G>A	XP_011514615.2:p.Ala659Thr
XM_011516315.3:c.1045G>A	XP_011514617.2:p.Ala349Thr
XM_017012323.2:c.1705G>A	XP_016867812.1:p.Ala569Thr
XR_001744809.2:n.2476G>A
XR_001744810.2:n.2471G>A
NM_000443.4:c.1705G>A MANE Select	NP_000434.1:p.Ala569Thr
NM_018849.3:c.1705G>A	NP_061337.1:p.Ala569Thr
NM_018850.3:c.1705G>A	NP_061338.1:p.Ala569Thr