Canonical Allele Identifier: CA368056911

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031555G>T (hg19) ; chr7:g.87402239G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402239G>T , CM000669.2:g.87402239G>T	GRCh38
NC_000007.13:g.87031555G>T , CM000669.1:g.87031555G>T	GRCh37
NC_000007.12:g.86869491G>T	NCBI36
NG_007118.1:g.83194C>A
NG_007118.2:g.83194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3697C>A	ENSP00000352135.3:p.Leu1233Met
ENST00000649586.2:c.3697C>A MANE Select	ENSP00000496956.2:p.Leu1233Met
ENST00000265723.8:c.3718C>A	ENSP00000265723.4:p.Leu1240Met
ENST00000358400.7:c.3556C>A	ENSP00000351172.3:p.Leu1186Met
ENST00000359206.7:c.3697C>A	ENSP00000352135.3:p.Leu1233Met
ENST00000440025.1:c.131C>A
ENST00000453593.5:c.3556C>A	ENSP00000392983.1:p.Leu1186Met
ENST00000467983.1:n.309C>A
NM_000443.3:c.3697C>A	NP_000434.1:p.Leu1233Met
NM_018849.2:c.3718C>A	NP_061337.1:p.Leu1240Met
NM_018850.2:c.3556C>A	NP_061338.1:p.Leu1186Met
XM_011516308.1:c.3718C>A	XP_011514610.1:p.Leu1240Met
XM_011516309.1:c.3697C>A	XP_011514611.1:p.Leu1233Met
XM_011516310.1:c.3613C>A	XP_011514612.1:p.Leu1205Met
XM_011516311.1:c.3589C>A	XP_011514613.1:p.Leu1197Met
XM_011516312.1:c.3577C>A	XP_011514614.1:p.Leu1193Met
XM_011516313.1:c.3556C>A	XP_011514615.1:p.Leu1186Met
XM_011516314.1:c.3739C>A	XP_011514616.1:p.Leu1247Met
XM_011516315.1:c.3058C>A	XP_011514617.1:p.Leu1020Met
XM_011516308.3:c.3988C>A	XP_011514610.3:p.Leu1330Met
XM_011516309.3:c.3967C>A	XP_011514611.3:p.Leu1323Met
XM_011516310.3:c.3883C>A	XP_011514612.3:p.Leu1295Met
XM_011516311.3:c.3859C>A	XP_011514613.3:p.Leu1287Met
XM_011516312.3:c.3847C>A	XP_011514614.3:p.Leu1283Met
XM_011516313.3:c.3826C>A	XP_011514615.2:p.Leu1276Met
XM_011516315.3:c.3058C>A	XP_011514617.2:p.Leu1020Met
XM_017012323.2:c.3718C>A	XP_016867812.1:p.Leu1240Met
XR_001744809.2:n.4226C>A
NM_000443.4:c.3697C>A MANE Select	NP_000434.1:p.Leu1233Met
NM_018849.3:c.3718C>A	NP_061337.1:p.Leu1240Met
NM_018850.3:c.3556C>A	NP_061338.1:p.Leu1186Met