Canonical Allele Identifier: CA456349306
Gene: ABCB1 HGNC NCBI

Linked Data

gnomAD v4: 7-87515264-C-T
MyVariant Identifiers: chr7:g.87144580C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515264C>T , CM000669.2:g.87515264C>T GRCh38
NC_000007.13:g.87144580C>T , CM000669.1:g.87144580C>T GRCh37
NC_000007.12:g.86982516C>T NCBI36
NG_011513.1:g.202985G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3249G>A ENSP00000265724.3:p.Leu1083=
ENST00000622132.5:c.3249G>A MANE Select ENSP00000478255.1:p.Leu1083=
ENST00000265724.7:c.3249G>A ENSP00000265724.3:p.Leu1083=
ENST00000475929.5:n.405G>A
ENST00000488737.6:n.891G>A
ENST00000496821.5:n.877G>A
ENST00000543898.5:c.3057G>A ENSP00000444095.1:p.Leu1019=
ENST00000622132.4:c.3249G>A ENSP00000478255.1:p.Leu1083=
NM_000927.4:c.3249G>A NP_000918.2:p.Leu1083=
NM_001348944.1:c.3249G>A NP_001335873.1:p.Leu1083=
NM_001348945.1:c.3459G>A NP_001335874.1:p.Leu1153=
NM_001348946.1:c.3249G>A NP_001335875.1:p.Leu1083=
NM_001348946.2:c.3249G>A MANE Select NP_001335875.1:p.Leu1083=
NM_000927.5:c.3249G>A NP_000918.2:p.Leu1083=
NM_001348944.2:c.3249G>A NP_001335873.1:p.Leu1083=
NM_001348945.2:c.3459G>A NP_001335874.1:p.Leu1153=