Canonical Allele Identifier: CA456349790

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87145912G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516596G>T , CM000669.2:g.87516596G>T	GRCh38
NC_000007.13:g.87145912G>T , CM000669.1:g.87145912G>T	GRCh37
NC_000007.12:g.86983848G>T	NCBI36
NG_011513.1:g.201653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2997C>A	ENSP00000265724.3:p.Ala999=
ENST00000622132.5:c.2997C>A MANE Select	ENSP00000478255.1:p.Ala999=
ENST00000265724.7:c.2997C>A	ENSP00000265724.3:p.Ala999=
ENST00000475929.5:n.153C>A
ENST00000483831.1:n.555C>A
ENST00000488737.6:n.639C>A
ENST00000496821.5:n.625C>A
ENST00000543898.5:c.2805C>A	ENSP00000444095.1:p.Ala935=
ENST00000622132.4:c.2997C>A	ENSP00000478255.1:p.Ala999=
NM_000927.4:c.2997C>A	NP_000918.2:p.Ala999=
NM_001348944.1:c.2997C>A	NP_001335873.1:p.Ala999=
NM_001348945.1:c.3207C>A	NP_001335874.1:p.Ala1069=
NM_001348946.1:c.2997C>A	NP_001335875.1:p.Ala999=
NM_001348946.2:c.2997C>A MANE Select	NP_001335875.1:p.Ala999=
NM_000927.5:c.2997C>A	NP_000918.2:p.Ala999=
NM_001348944.2:c.2997C>A	NP_001335873.1:p.Ala999=
NM_001348945.2:c.3207C>A	NP_001335874.1:p.Ala1069=