Canonical Allele Identifier: CA368056815

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031533T>A (hg19) ; chr7:g.87402217T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402217T>A , CM000669.2:g.87402217T>A	GRCh38
NC_000007.13:g.87031533T>A , CM000669.1:g.87031533T>A	GRCh37
NC_000007.12:g.86869469T>A	NCBI36
NG_007118.1:g.83216A>T
NG_007118.2:g.83216A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3719A>T	ENSP00000352135.3:p.Asp1240Val
ENST00000649586.2:c.3719A>T MANE Select	ENSP00000496956.2:p.Asp1240Val
ENST00000265723.8:c.3740A>T	ENSP00000265723.4:p.Asp1247Val
ENST00000358400.7:c.3578A>T	ENSP00000351172.3:p.Asp1193Val
ENST00000359206.7:c.3719A>T	ENSP00000352135.3:p.Asp1240Val
ENST00000440025.1:c.153A>T
ENST00000453593.5:c.3578A>T	ENSP00000392983.1:p.Asp1193Val
ENST00000467983.1:n.331A>T
NM_000443.3:c.3719A>T	NP_000434.1:p.Asp1240Val
NM_018849.2:c.3740A>T	NP_061337.1:p.Asp1247Val
NM_018850.2:c.3578A>T	NP_061338.1:p.Asp1193Val
XM_011516308.1:c.3740A>T	XP_011514610.1:p.Asp1247Val
XM_011516309.1:c.3719A>T	XP_011514611.1:p.Asp1240Val
XM_011516310.1:c.3635A>T	XP_011514612.1:p.Asp1212Val
XM_011516311.1:c.3611A>T	XP_011514613.1:p.Asp1204Val
XM_011516312.1:c.3599A>T	XP_011514614.1:p.Asp1200Val
XM_011516313.1:c.3578A>T	XP_011514615.1:p.Asp1193Val
XM_011516314.1:c.3761A>T	XP_011514616.1:p.Asp1254Val
XM_011516315.1:c.3080A>T	XP_011514617.1:p.Asp1027Val
XM_011516308.3:c.4010A>T	XP_011514610.3:p.Asp1337Val
XM_011516309.3:c.3989A>T	XP_011514611.3:p.Asp1330Val
XM_011516310.3:c.3905A>T	XP_011514612.3:p.Asp1302Val
XM_011516311.3:c.3881A>T	XP_011514613.3:p.Asp1294Val
XM_011516312.3:c.3869A>T	XP_011514614.3:p.Asp1290Val
XM_011516313.3:c.3848A>T	XP_011514615.2:p.Asp1283Val
XM_011516315.3:c.3080A>T	XP_011514617.2:p.Asp1027Val
XM_017012323.2:c.3740A>T	XP_016867812.1:p.Asp1247Val
XR_001744809.2:n.4248A>T
NM_000443.4:c.3719A>T MANE Select	NP_000434.1:p.Asp1240Val
NM_018849.3:c.3740A>T	NP_061337.1:p.Asp1247Val
NM_018850.3:c.3578A>T	NP_061338.1:p.Asp1193Val