Canonical Allele Identifier: CA456357183
Gene: ABCB1 HGNC NCBI

Linked Data

gnomAD v4: 7-87536473-A-G
MyVariant Identifiers: chr7:g.87165789A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87536473A>G , CM000669.2:g.87536473A>G GRCh38
NC_000007.13:g.87165789A>G , CM000669.1:g.87165789A>G GRCh37
NC_000007.12:g.87003725A>G NCBI36
NG_011513.1:g.181776T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2466T>C ENSP00000265724.3:p.Ala822=
ENST00000622132.5:c.2466T>C MANE Select ENSP00000478255.1:p.Ala822=
ENST00000265724.7:c.2466T>C ENSP00000265724.3:p.Ala822=
ENST00000496821.5:n.94T>C
ENST00000543898.5:c.2274T>C ENSP00000444095.1:p.Ala758=
ENST00000622132.4:c.2466T>C ENSP00000478255.1:p.Ala822=
NM_000927.4:c.2466T>C NP_000918.2:p.Ala822=
NM_001348944.1:c.2466T>C NP_001335873.1:p.Ala822=
NM_001348945.1:c.2676T>C NP_001335874.1:p.Ala892=
NM_001348946.1:c.2466T>C NP_001335875.1:p.Ala822=
NM_001348946.2:c.2466T>C MANE Select NP_001335875.1:p.Ala822=
NM_000927.5:c.2466T>C NP_000918.2:p.Ala822=
NM_001348944.2:c.2466T>C NP_001335873.1:p.Ala822=
NM_001348945.2:c.2676T>C NP_001335874.1:p.Ala892=