Canonical Allele Identifier: CA368056708

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031491C>A (hg19) ; chr7:g.87402175C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402175C>A , CM000669.2:g.87402175C>A	GRCh38
NC_000007.13:g.87031491C>A , CM000669.1:g.87031491C>A	GRCh37
NC_000007.12:g.86869427C>A	NCBI36
NG_007118.1:g.83258G>T
NG_007118.2:g.83258G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3761G>T	ENSP00000352135.3:p.Gly1254Val
ENST00000649586.2:c.3761G>T MANE Select	ENSP00000496956.2:p.Gly1254Val
ENST00000265723.8:c.3782G>T	ENSP00000265723.4:p.Gly1261Val
ENST00000358400.7:c.3620G>T	ENSP00000351172.3:p.Gly1207Val
ENST00000359206.7:c.3761G>T	ENSP00000352135.3:p.Gly1254Val
ENST00000440025.1:c.195G>T
ENST00000453593.5:c.3620G>T	ENSP00000392983.1:p.Gly1207Val
ENST00000467983.1:n.373G>T
NM_000443.3:c.3761G>T	NP_000434.1:p.Gly1254Val
NM_018849.2:c.3782G>T	NP_061337.1:p.Gly1261Val
NM_018850.2:c.3620G>T	NP_061338.1:p.Gly1207Val
XM_011516308.1:c.3782G>T	XP_011514610.1:p.Gly1261Val
XM_011516309.1:c.3761G>T	XP_011514611.1:p.Gly1254Val
XM_011516310.1:c.3677G>T	XP_011514612.1:p.Gly1226Val
XM_011516311.1:c.3653G>T	XP_011514613.1:p.Gly1218Val
XM_011516312.1:c.3641G>T	XP_011514614.1:p.Gly1214Val
XM_011516313.1:c.3620G>T	XP_011514615.1:p.Gly1207Val
XM_011516314.1:c.3803G>T	XP_011514616.1:p.Gly1268Val
XM_011516315.1:c.3122G>T	XP_011514617.1:p.Gly1041Val
XM_011516308.3:c.4052G>T	XP_011514610.3:p.Gly1351Val
XM_011516309.3:c.4031G>T	XP_011514611.3:p.Gly1344Val
XM_011516310.3:c.3947G>T	XP_011514612.3:p.Gly1316Val
XM_011516311.3:c.3923G>T	XP_011514613.3:p.Gly1308Val
XM_011516312.3:c.3911G>T	XP_011514614.3:p.Gly1304Val
XM_011516313.3:c.3890G>T	XP_011514615.2:p.Gly1297Val
XM_011516315.3:c.3122G>T	XP_011514617.2:p.Gly1041Val
XM_017012323.2:c.3782G>T	XP_016867812.1:p.Gly1261Val
XR_001744809.2:n.4290G>T
NM_000443.4:c.3761G>T MANE Select	NP_000434.1:p.Gly1254Val
NM_018849.3:c.3782G>T	NP_061337.1:p.Gly1261Val
NM_018850.3:c.3620G>T	NP_061338.1:p.Gly1207Val