Canonical Allele Identifier: CA368056833

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031537C>T (hg19) ; chr7:g.87402221C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402221C>T , CM000669.2:g.87402221C>T	GRCh38
NC_000007.13:g.87031537C>T , CM000669.1:g.87031537C>T	GRCh37
NC_000007.12:g.86869473C>T	NCBI36
NG_007118.1:g.83212G>A
NG_007118.2:g.83212G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3715G>A	ENSP00000352135.3:p.Ala1239Thr
ENST00000649586.2:c.3715G>A MANE Select	ENSP00000496956.2:p.Ala1239Thr
ENST00000265723.8:c.3736G>A	ENSP00000265723.4:p.Ala1246Thr
ENST00000358400.7:c.3574G>A	ENSP00000351172.3:p.Ala1192Thr
ENST00000359206.7:c.3715G>A	ENSP00000352135.3:p.Ala1239Thr
ENST00000440025.1:c.149G>A
ENST00000453593.5:c.3574G>A	ENSP00000392983.1:p.Ala1192Thr
ENST00000467983.1:n.327G>A
NM_000443.3:c.3715G>A	NP_000434.1:p.Ala1239Thr
NM_018849.2:c.3736G>A	NP_061337.1:p.Ala1246Thr
NM_018850.2:c.3574G>A	NP_061338.1:p.Ala1192Thr
XM_011516308.1:c.3736G>A	XP_011514610.1:p.Ala1246Thr
XM_011516309.1:c.3715G>A	XP_011514611.1:p.Ala1239Thr
XM_011516310.1:c.3631G>A	XP_011514612.1:p.Ala1211Thr
XM_011516311.1:c.3607G>A	XP_011514613.1:p.Ala1203Thr
XM_011516312.1:c.3595G>A	XP_011514614.1:p.Ala1199Thr
XM_011516313.1:c.3574G>A	XP_011514615.1:p.Ala1192Thr
XM_011516314.1:c.3757G>A	XP_011514616.1:p.Ala1253Thr
XM_011516315.1:c.3076G>A	XP_011514617.1:p.Ala1026Thr
XM_011516308.3:c.4006G>A	XP_011514610.3:p.Ala1336Thr
XM_011516309.3:c.3985G>A	XP_011514611.3:p.Ala1329Thr
XM_011516310.3:c.3901G>A	XP_011514612.3:p.Ala1301Thr
XM_011516311.3:c.3877G>A	XP_011514613.3:p.Ala1293Thr
XM_011516312.3:c.3865G>A	XP_011514614.3:p.Ala1289Thr
XM_011516313.3:c.3844G>A	XP_011514615.2:p.Ala1282Thr
XM_011516315.3:c.3076G>A	XP_011514617.2:p.Ala1026Thr
XM_017012323.2:c.3736G>A	XP_016867812.1:p.Ala1246Thr
XR_001744809.2:n.4244G>A
NM_000443.4:c.3715G>A MANE Select	NP_000434.1:p.Ala1239Thr
NM_018849.3:c.3736G>A	NP_061337.1:p.Ala1246Thr
NM_018850.3:c.3574G>A	NP_061338.1:p.Ala1192Thr