Canonical Allele Identifier: CA368056869

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031545A>G (hg19) ; chr7:g.87402229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402229A>G , CM000669.2:g.87402229A>G	GRCh38
NC_000007.13:g.87031545A>G , CM000669.1:g.87031545A>G	GRCh37
NC_000007.12:g.86869481A>G	NCBI36
NG_007118.1:g.83204T>C
NG_007118.2:g.83204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3707T>C	ENSP00000352135.3:p.Ile1236Thr
ENST00000649586.2:c.3707T>C MANE Select	ENSP00000496956.2:p.Ile1236Thr
ENST00000265723.8:c.3728T>C	ENSP00000265723.4:p.Ile1243Thr
ENST00000358400.7:c.3566T>C	ENSP00000351172.3:p.Ile1189Thr
ENST00000359206.7:c.3707T>C	ENSP00000352135.3:p.Ile1236Thr
ENST00000440025.1:c.141T>C
ENST00000453593.5:c.3566T>C	ENSP00000392983.1:p.Ile1189Thr
ENST00000467983.1:n.319T>C
NM_000443.3:c.3707T>C	NP_000434.1:p.Ile1236Thr
NM_018849.2:c.3728T>C	NP_061337.1:p.Ile1243Thr
NM_018850.2:c.3566T>C	NP_061338.1:p.Ile1189Thr
XM_011516308.1:c.3728T>C	XP_011514610.1:p.Ile1243Thr
XM_011516309.1:c.3707T>C	XP_011514611.1:p.Ile1236Thr
XM_011516310.1:c.3623T>C	XP_011514612.1:p.Ile1208Thr
XM_011516311.1:c.3599T>C	XP_011514613.1:p.Ile1200Thr
XM_011516312.1:c.3587T>C	XP_011514614.1:p.Ile1196Thr
XM_011516313.1:c.3566T>C	XP_011514615.1:p.Ile1189Thr
XM_011516314.1:c.3749T>C	XP_011514616.1:p.Ile1250Thr
XM_011516315.1:c.3068T>C	XP_011514617.1:p.Ile1023Thr
XM_011516308.3:c.3998T>C	XP_011514610.3:p.Ile1333Thr
XM_011516309.3:c.3977T>C	XP_011514611.3:p.Ile1326Thr
XM_011516310.3:c.3893T>C	XP_011514612.3:p.Ile1298Thr
XM_011516311.3:c.3869T>C	XP_011514613.3:p.Ile1290Thr
XM_011516312.3:c.3857T>C	XP_011514614.3:p.Ile1286Thr
XM_011516313.3:c.3836T>C	XP_011514615.2:p.Ile1279Thr
XM_011516315.3:c.3068T>C	XP_011514617.2:p.Ile1023Thr
XM_017012323.2:c.3728T>C	XP_016867812.1:p.Ile1243Thr
XR_001744809.2:n.4236T>C
NM_000443.4:c.3707T>C MANE Select	NP_000434.1:p.Ile1236Thr
NM_018849.3:c.3728T>C	NP_061337.1:p.Ile1243Thr
NM_018850.3:c.3566T>C	NP_061338.1:p.Ile1189Thr