Canonical Allele Identifier: CA456349305
Gene: ABCB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.87144580C>G (hg19)

Genomic Alleles

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

Transcript Alleles

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