Canonical Allele Identifier: CA413678892

Gene: ABCB7

Linked Data

• MyVariant Identifiers: chrX:g.74375987A>T (hg19) ; chrX:g.75156152A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.75156152A>T , CM000685.2:g.75156152A>T	GRCh38
NC_000023.10:g.74375987A>T , CM000685.1:g.74375987A>T	GRCh37
NC_000023.9:g.74292712A>T	NCBI36
NG_007980.1:g.5146T>A
NG_007980.3:g.5132T>A
NG_015972.2:g.4774A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253577.9:c.121T>A	ENSP00000253577.3:p.Trp41Arg
ENST00000373394.8:c.121T>A MANE Select	ENSP00000362492.3:p.Trp41Arg
ENST00000526404.2:c.121T>A	ENSP00000432813.2:p.Trp41Arg
ENST00000620875.5:c.121T>A	ENSP00000479985.1:p.Trp41Arg
ENST00000643632.1:c.131T>A
ENST00000644766.1:c.121T>A	ENSP00000493713.1:p.Trp41Arg
ENST00000645829.3:c.121T>A	ENSP00000496526.2:p.Trp41Arg
ENST00000669573.1:c.121T>A	ENSP00000499543.1:p.Trp41Arg
ENST00000253577.7:c.121T>A	ENSP00000253577.3:p.Trp41Arg
ENST00000339447.8:c.121T>A	ENSP00000343849.4:p.Trp41Arg
ENST00000373394.7:c.121T>A	ENSP00000362492.3:p.Trp41Arg
ENST00000526404.1:c.157T>A	ENSP00000432813.1:p.Trp53Arg
ENST00000529949.5:c.121T>A	ENSP00000436586.1:p.Trp41Arg
ENST00000534524.5:c.121T>A	ENSP00000435521.1:p.Trp41Arg
ENST00000620875.4:c.121T>A	ENSP00000479985.1:p.Trp41Arg
NM_001271696.1:c.121T>A	NP_001258625.1:p.Trp41Arg
NM_001271697.1:c.121T>A	NP_001258626.1:p.Trp41Arg
NM_001271698.1:c.121T>A	NP_001258627.1:p.Trp41Arg
NM_001271699.1:c.121T>A	NP_001258628.1:p.Trp41Arg
NM_004299.4:c.121T>A	NP_004290.2:p.Trp41Arg
NM_001271696.2:c.121T>A	NP_001258625.1:p.Trp41Arg
NM_001271697.2:c.121T>A	NP_001258626.1:p.Trp41Arg
NM_001271698.2:c.121T>A	NP_001258627.1:p.Trp41Arg
NM_001271699.2:c.121T>A	NP_001258628.1:p.Trp41Arg
NM_004299.6:c.121T>A	NP_004290.2:p.Trp41Arg
NM_001271696.3:c.121T>A MANE Select	NP_001258625.1:p.Trp41Arg
NM_001271697.3:c.121T>A	NP_001258626.1:p.Trp41Arg
NM_001271698.3:c.121T>A	NP_001258627.1:p.Trp41Arg
NM_001271699.3:c.121T>A	NP_001258628.1:p.Trp41Arg