Canonical Allele Identifier: CA4328715
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs760162850
gnomAD v2: 7-87229450-A-T
gnomAD v3: 7-87600134-A-T
gnomAD v4: 7-87600134-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600134A>T , CM000669.2:g.87600134A>T GRCh38
NC_000007.13:g.87229450A>T , CM000669.1:g.87229450A>T GRCh37
NC_000007.12:g.87067386A>T NCBI36
NG_011513.1:g.118115T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.51T>A ENSP00000265724.3:p.Phe17Leu
ENST00000622132.5:c.51T>A MANE Select ENSP00000478255.1:p.Phe17Leu
ENST00000265724.7:c.51T>A ENSP00000265724.3:p.Phe17Leu
ENST00000416177.1:c.51T>A ENSP00000399419.1:p.Phe17Leu
ENST00000543898.5:c.51T>A ENSP00000444095.1:p.Phe17Leu
ENST00000622132.4:c.51T>A ENSP00000478255.1:p.Phe17Leu
NM_000927.4:c.51T>A NP_000918.2:p.Phe17Leu
NM_001348944.1:c.51T>A NP_001335873.1:p.Phe17Leu
NM_001348945.1:c.261T>A NP_001335874.1:p.Phe87Leu
NM_001348946.1:c.51T>A NP_001335875.1:p.Phe17Leu
NM_001348946.2:c.51T>A MANE Select NP_001335875.1:p.Phe17Leu
NM_000927.5:c.51T>A NP_000918.2:p.Phe17Leu
NM_001348944.2:c.51T>A NP_001335873.1:p.Phe17Leu
NM_001348945.2:c.261T>A NP_001335874.1:p.Phe87Leu