Canonical Allele Identifier: CA368056843

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031539T>G (hg19) ; chr7:g.87402223T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402223T>G , CM000669.2:g.87402223T>G	GRCh38
NC_000007.13:g.87031539T>G , CM000669.1:g.87031539T>G	GRCh37
NC_000007.12:g.86869475T>G	NCBI36
NG_007118.1:g.83210A>C
NG_007118.2:g.83210A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3713A>C	ENSP00000352135.3:p.Asn1238Thr
ENST00000649586.2:c.3713A>C MANE Select	ENSP00000496956.2:p.Asn1238Thr
ENST00000265723.8:c.3734A>C	ENSP00000265723.4:p.Asn1245Thr
ENST00000358400.7:c.3572A>C	ENSP00000351172.3:p.Asn1191Thr
ENST00000359206.7:c.3713A>C	ENSP00000352135.3:p.Asn1238Thr
ENST00000440025.1:c.147A>C
ENST00000453593.5:c.3572A>C	ENSP00000392983.1:p.Asn1191Thr
ENST00000467983.1:n.325A>C
NM_000443.3:c.3713A>C	NP_000434.1:p.Asn1238Thr
NM_018849.2:c.3734A>C	NP_061337.1:p.Asn1245Thr
NM_018850.2:c.3572A>C	NP_061338.1:p.Asn1191Thr
XM_011516308.1:c.3734A>C	XP_011514610.1:p.Asn1245Thr
XM_011516309.1:c.3713A>C	XP_011514611.1:p.Asn1238Thr
XM_011516310.1:c.3629A>C	XP_011514612.1:p.Asn1210Thr
XM_011516311.1:c.3605A>C	XP_011514613.1:p.Asn1202Thr
XM_011516312.1:c.3593A>C	XP_011514614.1:p.Asn1198Thr
XM_011516313.1:c.3572A>C	XP_011514615.1:p.Asn1191Thr
XM_011516314.1:c.3755A>C	XP_011514616.1:p.Asn1252Thr
XM_011516315.1:c.3074A>C	XP_011514617.1:p.Asn1025Thr
XM_011516308.3:c.4004A>C	XP_011514610.3:p.Asn1335Thr
XM_011516309.3:c.3983A>C	XP_011514611.3:p.Asn1328Thr
XM_011516310.3:c.3899A>C	XP_011514612.3:p.Asn1300Thr
XM_011516311.3:c.3875A>C	XP_011514613.3:p.Asn1292Thr
XM_011516312.3:c.3863A>C	XP_011514614.3:p.Asn1288Thr
XM_011516313.3:c.3842A>C	XP_011514615.2:p.Asn1281Thr
XM_011516315.3:c.3074A>C	XP_011514617.2:p.Asn1025Thr
XM_017012323.2:c.3734A>C	XP_016867812.1:p.Asn1245Thr
XR_001744809.2:n.4242A>C
NM_000443.4:c.3713A>C MANE Select	NP_000434.1:p.Asn1238Thr
NM_018849.3:c.3734A>C	NP_061337.1:p.Asn1245Thr
NM_018850.3:c.3572A>C	NP_061338.1:p.Asn1191Thr