Canonical Allele Identifier: CA2683610161
Gene: ABCB1 HGNC NCBI

Linked Data

gnomAD v4: 7-87601003-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87601003T>C , CM000669.2:g.87601003T>C GRCh38
NC_000007.13:g.87230319T>C , CM000669.1:g.87230319T>C GRCh37
NC_000007.12:g.87068255T>C NCBI36
NG_011513.1:g.117246A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.-255A>G ENSP00000265724.3:n.-255A>G
ENST00000265724.7:c.-255A>G ENSP00000265724.3:n.-255A>G
ENST00000416177.1:c.-108A>G ENSP00000399419.1:n.-108A>G
ENST00000476862.1:n.392A>G
ENST00000543898.5:c.-255A>G ENSP00000444095.1:n.-255A>G
ENST00000622132.4:c.-255A>G ENSP00000478255.1:n.-255A>G
NM_000927.4:c.-255A>G NP_000918.2:n.-255A>G
NM_001348944.1:c.-108A>G NP_001335873.1:n.-108A>G
NM_001348945.1:c.103A>G NP_001335874.1:p.Ser35Gly
NM_000927.5:c.-255A>G NP_000918.2:n.-255A>G
NM_001348944.2:c.-108A>G NP_001335873.1:n.-108A>G
NM_001348945.2:c.103A>G NP_001335874.1:p.Ser35Gly