Canonical Allele Identifier: CA1104126362
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1816037841
gnomAD v3: 7-87531138-A-T
gnomAD v4: 7-87531138-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87531138A>T , CM000669.2:g.87531138A>T GRCh38
NC_000007.13:g.87160454A>T , CM000669.1:g.87160454A>T GRCh37
NC_000007.12:g.86998390A>T NCBI36
NG_011513.1:g.187111T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.2685+156T>A ENSP00000265724.3:n.2685+156T>A
ENST00000622132.5:c.2685+156T>A MANE Select ENSP00000478255.1:n.2685+156T>A
ENST00000265724.7:c.2685+156T>A ENSP00000265724.3:n.2685+156T>A
ENST00000488737.6:n.327+156T>A
ENST00000496821.5:n.313+156T>A
ENST00000543898.5:c.2493+156T>A ENSP00000444095.1:n.2493+156T>A
ENST00000622132.4:c.2685+156T>A ENSP00000478255.1:n.2685+156T>A
NM_000927.4:c.2685+156T>A NP_000918.2:n.2685+156T>A
NM_001348944.1:c.2685+156T>A NP_001335873.1:n.2685+156T>A
NM_001348945.1:c.2895+156T>A NP_001335874.1:n.2895+156T>A
NM_001348946.1:c.2685+156T>A NP_001335875.1:n.2685+156T>A
NM_001348946.2:c.2685+156T>A MANE Select NP_001335875.1:n.2685+156T>A
NM_000927.5:c.2685+156T>A NP_000918.2:n.2685+156T>A
NM_001348944.2:c.2685+156T>A NP_001335873.1:n.2685+156T>A
NM_001348945.2:c.2895+156T>A NP_001335874.1:n.2895+156T>A