Canonical Allele Identifier: CA368062376
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550012A>G , CM000669.2:g.87550012A>G GRCh38
NC_000007.13:g.87179328A>G , CM000669.1:g.87179328A>G GRCh37
NC_000007.12:g.87017264A>G NCBI36
NG_011513.1:g.168237T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1393T>C ENSP00000265724.3:p.Phe465Leu
ENST00000622132.5:c.1393T>C MANE Select ENSP00000478255.1:p.Phe465Leu
ENST00000265724.7:c.1393T>C ENSP00000265724.3:p.Phe465Leu
ENST00000482527.1:n.147T>C
ENST00000543898.5:c.1201T>C ENSP00000444095.1:p.Phe401Leu
ENST00000622132.4:c.1393T>C ENSP00000478255.1:p.Phe465Leu
NM_000927.4:c.1393T>C NP_000918.2:p.Phe465Leu
NM_001348944.1:c.1393T>C NP_001335873.1:p.Phe465Leu
NM_001348945.1:c.1603T>C NP_001335874.1:p.Phe535Leu
NM_001348946.1:c.1393T>C NP_001335875.1:p.Phe465Leu
NM_001348946.2:c.1393T>C MANE Select NP_001335875.1:p.Phe465Leu
NM_000927.5:c.1393T>C NP_000918.2:p.Phe465Leu
NM_001348944.2:c.1393T>C NP_001335873.1:p.Phe465Leu
NM_001348945.2:c.1603T>C NP_001335874.1:p.Phe535Leu