Canonical Allele Identifier: CA368056811

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031532G>C (hg19) ; chr7:g.87402216G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402216G>C , CM000669.2:g.87402216G>C	GRCh38
NC_000007.13:g.87031532G>C , CM000669.1:g.87031532G>C	GRCh37
NC_000007.12:g.86869468G>C	NCBI36
NG_007118.1:g.83217C>G
NG_007118.2:g.83217C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3720C>G	ENSP00000352135.3:p.Asp1240Glu
ENST00000649586.2:c.3720C>G MANE Select	ENSP00000496956.2:p.Asp1240Glu
ENST00000265723.8:c.3741C>G	ENSP00000265723.4:p.Asp1247Glu
ENST00000358400.7:c.3579C>G	ENSP00000351172.3:p.Asp1193Glu
ENST00000359206.7:c.3720C>G	ENSP00000352135.3:p.Asp1240Glu
ENST00000440025.1:c.154C>G
ENST00000453593.5:c.3579C>G	ENSP00000392983.1:p.Asp1193Glu
ENST00000467983.1:n.332C>G
NM_000443.3:c.3720C>G	NP_000434.1:p.Asp1240Glu
NM_018849.2:c.3741C>G	NP_061337.1:p.Asp1247Glu
NM_018850.2:c.3579C>G	NP_061338.1:p.Asp1193Glu
XM_011516308.1:c.3741C>G	XP_011514610.1:p.Asp1247Glu
XM_011516309.1:c.3720C>G	XP_011514611.1:p.Asp1240Glu
XM_011516310.1:c.3636C>G	XP_011514612.1:p.Asp1212Glu
XM_011516311.1:c.3612C>G	XP_011514613.1:p.Asp1204Glu
XM_011516312.1:c.3600C>G	XP_011514614.1:p.Asp1200Glu
XM_011516313.1:c.3579C>G	XP_011514615.1:p.Asp1193Glu
XM_011516314.1:c.3762C>G	XP_011514616.1:p.Asp1254Glu
XM_011516315.1:c.3081C>G	XP_011514617.1:p.Asp1027Glu
XM_011516308.3:c.4011C>G	XP_011514610.3:p.Asp1337Glu
XM_011516309.3:c.3990C>G	XP_011514611.3:p.Asp1330Glu
XM_011516310.3:c.3906C>G	XP_011514612.3:p.Asp1302Glu
XM_011516311.3:c.3882C>G	XP_011514613.3:p.Asp1294Glu
XM_011516312.3:c.3870C>G	XP_011514614.3:p.Asp1290Glu
XM_011516313.3:c.3849C>G	XP_011514615.2:p.Asp1283Glu
XM_011516315.3:c.3081C>G	XP_011514617.2:p.Asp1027Glu
XM_017012323.2:c.3741C>G	XP_016867812.1:p.Asp1247Glu
XR_001744809.2:n.4249C>G
NM_000443.4:c.3720C>G MANE Select	NP_000434.1:p.Asp1240Glu
NM_018849.3:c.3741C>G	NP_061337.1:p.Asp1247Glu
NM_018850.3:c.3579C>G	NP_061338.1:p.Asp1193Glu