Canonical Allele Identifier: CA368056974

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031570C>G (hg19) ; chr7:g.87402254C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402254C>G , CM000669.2:g.87402254C>G	GRCh38
NC_000007.13:g.87031570C>G , CM000669.1:g.87031570C>G	GRCh37
NC_000007.12:g.86869506C>G	NCBI36
NG_007118.1:g.83179G>C
NG_007118.2:g.83179G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3682G>C	ENSP00000352135.3:p.Val1228Leu
ENST00000649586.2:c.3682G>C MANE Select	ENSP00000496956.2:p.Val1228Leu
ENST00000265723.8:c.3703G>C	ENSP00000265723.4:p.Val1235Leu
ENST00000358400.7:c.3541G>C	ENSP00000351172.3:p.Val1181Leu
ENST00000359206.7:c.3682G>C	ENSP00000352135.3:p.Val1228Leu
ENST00000440025.1:c.116G>C
ENST00000453593.5:c.3541G>C	ENSP00000392983.1:p.Val1181Leu
ENST00000467983.1:n.294G>C
NM_000443.3:c.3682G>C	NP_000434.1:p.Val1228Leu
NM_018849.2:c.3703G>C	NP_061337.1:p.Val1235Leu
NM_018850.2:c.3541G>C	NP_061338.1:p.Val1181Leu
XM_011516308.1:c.3703G>C	XP_011514610.1:p.Val1235Leu
XM_011516309.1:c.3682G>C	XP_011514611.1:p.Val1228Leu
XM_011516310.1:c.3598G>C	XP_011514612.1:p.Val1200Leu
XM_011516311.1:c.3574G>C	XP_011514613.1:p.Val1192Leu
XM_011516312.1:c.3562G>C	XP_011514614.1:p.Val1188Leu
XM_011516313.1:c.3541G>C	XP_011514615.1:p.Val1181Leu
XM_011516314.1:c.3724G>C	XP_011514616.1:p.Val1242Leu
XM_011516315.1:c.3043G>C	XP_011514617.1:p.Val1015Leu
XM_011516308.3:c.3973G>C	XP_011514610.3:p.Val1325Leu
XM_011516309.3:c.3952G>C	XP_011514611.3:p.Val1318Leu
XM_011516310.3:c.3868G>C	XP_011514612.3:p.Val1290Leu
XM_011516311.3:c.3844G>C	XP_011514613.3:p.Val1282Leu
XM_011516312.3:c.3832G>C	XP_011514614.3:p.Val1278Leu
XM_011516313.3:c.3811G>C	XP_011514615.2:p.Val1271Leu
XM_011516315.3:c.3043G>C	XP_011514617.2:p.Val1015Leu
XM_017012323.2:c.3703G>C	XP_016867812.1:p.Val1235Leu
XR_001744809.2:n.4211G>C
NM_000443.4:c.3682G>C MANE Select	NP_000434.1:p.Val1228Leu
NM_018849.3:c.3703G>C	NP_061337.1:p.Val1235Leu
NM_018850.3:c.3541G>C	NP_061338.1:p.Val1181Leu