Canonical Allele Identifier: CA456349673

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87144724G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515408G>T , CM000669.2:g.87515408G>T	GRCh38
NC_000007.13:g.87144724G>T , CM000669.1:g.87144724G>T	GRCh37
NC_000007.12:g.86982660G>T	NCBI36
NG_011513.1:g.202841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3105C>A	ENSP00000265724.3:p.Val1035=
ENST00000622132.5:c.3105C>A MANE Select	ENSP00000478255.1:p.Val1035=
ENST00000265724.7:c.3105C>A	ENSP00000265724.3:p.Val1035=
ENST00000475929.5:n.261C>A
ENST00000488737.6:n.747C>A
ENST00000496821.5:n.733C>A
ENST00000543898.5:c.2913C>A	ENSP00000444095.1:p.Val971=
ENST00000622132.4:c.3105C>A	ENSP00000478255.1:p.Val1035=
NM_000927.4:c.3105C>A	NP_000918.2:p.Val1035=
NM_001348944.1:c.3105C>A	NP_001335873.1:p.Val1035=
NM_001348945.1:c.3315C>A	NP_001335874.1:p.Val1105=
NM_001348946.1:c.3105C>A	NP_001335875.1:p.Val1035=
NM_001348946.2:c.3105C>A MANE Select	NP_001335875.1:p.Val1035=
NM_000927.5:c.3105C>A	NP_000918.2:p.Val1035=
NM_001348944.2:c.3105C>A	NP_001335873.1:p.Val1035=
NM_001348945.2:c.3315C>A	NP_001335874.1:p.Val1105=