Canonical Allele Identifier: CA368057041

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031588C>A (hg19) ; chr7:g.87402272C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402272C>A , CM000669.2:g.87402272C>A	GRCh38
NC_000007.13:g.87031588C>A , CM000669.1:g.87031588C>A	GRCh37
NC_000007.12:g.86869524C>A	NCBI36
NG_007118.1:g.83161G>T
NG_007118.2:g.83161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3664G>T	ENSP00000352135.3:p.Glu1222Ter
ENST00000649586.2:c.3664G>T MANE Select	ENSP00000496956.2:p.Glu1222Ter
ENST00000265723.8:c.3685G>T	ENSP00000265723.4:p.Glu1229Ter
ENST00000358400.7:c.3523G>T	ENSP00000351172.3:p.Glu1175Ter
ENST00000359206.7:c.3664G>T	ENSP00000352135.3:p.Glu1222Ter
ENST00000440025.1:c.98G>T
ENST00000453593.5:c.3523G>T	ENSP00000392983.1:p.Glu1175Ter
ENST00000467983.1:n.276G>T
NM_000443.3:c.3664G>T	NP_000434.1:p.Glu1222Ter
NM_018849.2:c.3685G>T	NP_061337.1:p.Glu1229Ter
NM_018850.2:c.3523G>T	NP_061338.1:p.Glu1175Ter
XM_011516308.1:c.3685G>T	XP_011514610.1:p.Glu1229Ter
XM_011516309.1:c.3664G>T	XP_011514611.1:p.Glu1222Ter
XM_011516310.1:c.3580G>T	XP_011514612.1:p.Glu1194Ter
XM_011516311.1:c.3556G>T	XP_011514613.1:p.Glu1186Ter
XM_011516312.1:c.3544G>T	XP_011514614.1:p.Glu1182Ter
XM_011516313.1:c.3523G>T	XP_011514615.1:p.Glu1175Ter
XM_011516314.1:c.3706G>T	XP_011514616.1:p.Glu1236Ter
XM_011516315.1:c.3025G>T	XP_011514617.1:p.Glu1009Ter
XM_011516308.3:c.3955G>T	XP_011514610.3:p.Glu1319Ter
XM_011516309.3:c.3934G>T	XP_011514611.3:p.Glu1312Ter
XM_011516310.3:c.3850G>T	XP_011514612.3:p.Glu1284Ter
XM_011516311.3:c.3826G>T	XP_011514613.3:p.Glu1276Ter
XM_011516312.3:c.3814G>T	XP_011514614.3:p.Glu1272Ter
XM_011516313.3:c.3793G>T	XP_011514615.2:p.Glu1265Ter
XM_011516315.3:c.3025G>T	XP_011514617.2:p.Glu1009Ter
XM_017012323.2:c.3685G>T	XP_016867812.1:p.Glu1229Ter
XR_001744809.2:n.4193G>T
NM_000443.4:c.3664G>T MANE Select	NP_000434.1:p.Glu1222Ter
NM_018849.3:c.3685G>T	NP_061337.1:p.Glu1229Ter
NM_018850.3:c.3523G>T	NP_061338.1:p.Glu1175Ter