Canonical Allele Identifier: CA4327115

Gene: ABCB4

Linked Data

• ClinVar Variation Id: 3023829
• ClinVar RCV Id: RCV003880924
• dbSNP Id: rs778345147
• ExAC: 7:87053297 G / A
• gnomAD v2: 7-87053297-G-A
• gnomAD v3: 7-87423981-G-A
• gnomAD v4: 7-87423981-G-A
• COSMIC: COSM3641892 ; COSM4891843
• MyVariant Identifiers: chr7:g.87053297G>A (hg19) ; chr7:g.87423981G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87423981G>A , CM000669.2:g.87423981G>A	GRCh38
NC_000007.13:g.87053297G>A , CM000669.1:g.87053297G>A	GRCh37
NC_000007.12:g.86891233G>A	NCBI36
NG_007118.1:g.61452C>T
NG_007118.2:g.61452C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.2136C>T	ENSP00000352135.3:p.Val712=
ENST00000643670.1:c.2152C>T	ENSP00000496629.1:n.2152C>T
ENST00000649586.2:c.2136C>T MANE Select	ENSP00000496956.2:p.Val712=
ENST00000265723.8:c.2136C>T	ENSP00000265723.4:p.Val712=
ENST00000358400.7:c.2136C>T	ENSP00000351172.3:p.Val712=
ENST00000359206.7:c.2136C>T	ENSP00000352135.3:p.Val712=
ENST00000453593.5:c.2136C>T	ENSP00000392983.1:p.Val712=
ENST00000469770.1:n.340C>T
NM_000443.3:c.2136C>T	NP_000434.1:p.Val712=
NM_018849.2:c.2136C>T	NP_061337.1:p.Val712=
NM_018850.2:c.2136C>T	NP_061338.1:p.Val712=
XM_011516308.1:c.2136C>T	XP_011514610.1:p.Val712=
XM_011516309.1:c.2136C>T	XP_011514611.1:p.Val712=
XM_011516310.1:c.2136C>T	XP_011514612.1:p.Val712=
XM_011516311.1:c.2136C>T	XP_011514613.1:p.Val712=
XM_011516312.1:c.2136C>T	XP_011514614.1:p.Val712=
XM_011516313.1:c.2136C>T	XP_011514615.1:p.Val712=
XM_011516314.1:c.2157C>T	XP_011514616.1:p.Val719=
XM_011516315.1:c.1476C>T	XP_011514617.1:p.Val492=
XR_927478.1:n.2232C>T
XM_011516308.3:c.2406C>T	XP_011514610.3:p.Val802=
XM_011516309.3:c.2406C>T	XP_011514611.3:p.Val802=
XM_011516310.3:c.2406C>T	XP_011514612.3:p.Val802=
XM_011516311.3:c.2406C>T	XP_011514613.3:p.Val802=
XM_011516312.3:c.2406C>T	XP_011514614.3:p.Val802=
XM_011516313.3:c.2406C>T	XP_011514615.2:p.Val802=
XM_011516315.3:c.1476C>T	XP_011514617.2:p.Val492=
XM_017012323.2:c.2136C>T	XP_016867812.1:p.Val712=
XR_001744809.2:n.2907C>T
XR_001744810.2:n.2902C>T
NM_000443.4:c.2136C>T MANE Select	NP_000434.1:p.Val712=
NM_018849.3:c.2136C>T	NP_061337.1:p.Val712=
NM_018850.3:c.2136C>T	NP_061338.1:p.Val712=