Canonical Allele Identifier: CA368050338

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150188G>A (hg19) ; chr7:g.87520872G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520872G>A , CM000669.2:g.87520872G>A	GRCh38
NC_000007.13:g.87150188G>A , CM000669.1:g.87150188G>A	GRCh37
NC_000007.12:g.86988124G>A	NCBI36
NG_011513.1:g.197377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2690C>T	ENSP00000265724.3:p.Ala897Val
ENST00000622132.5:c.2690C>T MANE Select	ENSP00000478255.1:p.Ala897Val
ENST00000265724.7:c.2690C>T	ENSP00000265724.3:p.Ala897Val
ENST00000483831.1:n.248C>T
ENST00000488737.6:n.332C>T
ENST00000496821.5:n.318C>T
ENST00000543898.5:c.2498C>T	ENSP00000444095.1:p.Ala833Val
ENST00000622132.4:c.2690C>T	ENSP00000478255.1:p.Ala897Val
NM_000927.4:c.2690C>T	NP_000918.2:p.Ala897Val
NM_001348944.1:c.2690C>T	NP_001335873.1:p.Ala897Val
NM_001348945.1:c.2900C>T	NP_001335874.1:p.Ala967Val
NM_001348946.1:c.2690C>T	NP_001335875.1:p.Ala897Val
NM_001348946.2:c.2690C>T MANE Select	NP_001335875.1:p.Ala897Val
NM_000927.5:c.2690C>T	NP_000918.2:p.Ala897Val
NM_001348944.2:c.2690C>T	NP_001335873.1:p.Ala897Val
NM_001348945.2:c.2900C>T	NP_001335874.1:p.Ala967Val