Canonical Allele Identifier: CA368062833
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550259T>A , CM000669.2:g.87550259T>A GRCh38
NC_000007.13:g.87179575T>A , CM000669.1:g.87179575T>A GRCh37
NC_000007.12:g.87017511T>A NCBI36
NG_011513.1:g.167990A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1262A>T ENSP00000265724.3:p.Gln421Leu
ENST00000622132.5:c.1262A>T MANE Select ENSP00000478255.1:p.Gln421Leu
ENST00000265724.7:c.1262A>T ENSP00000265724.3:p.Gln421Leu
ENST00000543898.5:c.1070A>T ENSP00000444095.1:p.Gln357Leu
ENST00000622132.4:c.1262A>T ENSP00000478255.1:p.Gln421Leu
NM_000927.4:c.1262A>T NP_000918.2:p.Gln421Leu
NM_001348944.1:c.1262A>T NP_001335873.1:p.Gln421Leu
NM_001348945.1:c.1472A>T NP_001335874.1:p.Gln491Leu
NM_001348946.1:c.1262A>T NP_001335875.1:p.Gln421Leu
NM_001348946.2:c.1262A>T MANE Select NP_001335875.1:p.Gln421Leu
NM_000927.5:c.1262A>T NP_000918.2:p.Gln421Leu
NM_001348944.2:c.1262A>T NP_001335873.1:p.Gln421Leu
NM_001348945.2:c.1472A>T NP_001335874.1:p.Gln491Leu