Canonical Allele Identifier: CA456356284

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031562A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402246A>C , CM000669.2:g.87402246A>C	GRCh38
NC_000007.13:g.87031562A>C , CM000669.1:g.87031562A>C	GRCh37
NC_000007.12:g.86869498A>C	NCBI36
NG_007118.1:g.83187T>G
NG_007118.2:g.83187T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3690T>G	ENSP00000352135.3:p.Ala1230=
ENST00000649586.2:c.3690T>G MANE Select	ENSP00000496956.2:p.Ala1230=
ENST00000265723.8:c.3711T>G	ENSP00000265723.4:p.Ala1237=
ENST00000358400.7:c.3549T>G	ENSP00000351172.3:p.Ala1183=
ENST00000359206.7:c.3690T>G	ENSP00000352135.3:p.Ala1230=
ENST00000440025.1:c.124T>G
ENST00000453593.5:c.3549T>G	ENSP00000392983.1:p.Ala1183=
ENST00000467983.1:n.302T>G
NM_000443.3:c.3690T>G	NP_000434.1:p.Ala1230=
NM_018849.2:c.3711T>G	NP_061337.1:p.Ala1237=
NM_018850.2:c.3549T>G	NP_061338.1:p.Ala1183=
XM_011516308.1:c.3711T>G	XP_011514610.1:p.Ala1237=
XM_011516309.1:c.3690T>G	XP_011514611.1:p.Ala1230=
XM_011516310.1:c.3606T>G	XP_011514612.1:p.Ala1202=
XM_011516311.1:c.3582T>G	XP_011514613.1:p.Ala1194=
XM_011516312.1:c.3570T>G	XP_011514614.1:p.Ala1190=
XM_011516313.1:c.3549T>G	XP_011514615.1:p.Ala1183=
XM_011516314.1:c.3732T>G	XP_011514616.1:p.Ala1244=
XM_011516315.1:c.3051T>G	XP_011514617.1:p.Ala1017=
XM_011516308.3:c.3981T>G	XP_011514610.3:p.Ala1327=
XM_011516309.3:c.3960T>G	XP_011514611.3:p.Ala1320=
XM_011516310.3:c.3876T>G	XP_011514612.3:p.Ala1292=
XM_011516311.3:c.3852T>G	XP_011514613.3:p.Ala1284=
XM_011516312.3:c.3840T>G	XP_011514614.3:p.Ala1280=
XM_011516313.3:c.3819T>G	XP_011514615.2:p.Ala1273=
XM_011516315.3:c.3051T>G	XP_011514617.2:p.Ala1017=
XM_017012323.2:c.3711T>G	XP_016867812.1:p.Ala1237=
XR_001744809.2:n.4219T>G
NM_000443.4:c.3690T>G MANE Select	NP_000434.1:p.Ala1230=
NM_018849.3:c.3711T>G	NP_061337.1:p.Ala1237=
NM_018850.3:c.3549T>G	NP_061338.1:p.Ala1183=