Canonical Allele Identifier: CA4328722
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs758755760
gnomAD v2: 7-87229482-G-C
gnomAD v4: 7-87600166-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600166G>C , CM000669.2:g.87600166G>C GRCh38
NC_000007.13:g.87229482G>C , CM000669.1:g.87229482G>C GRCh37
NC_000007.12:g.87067418G>C NCBI36
NG_011513.1:g.118083C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.19C>G ENSP00000265724.3:p.Arg7Gly
ENST00000622132.5:c.19C>G MANE Select ENSP00000478255.1:p.Arg7Gly
ENST00000265724.7:c.19C>G ENSP00000265724.3:p.Arg7Gly
ENST00000416177.1:c.19C>G ENSP00000399419.1:p.Arg7Gly
ENST00000543898.5:c.19C>G ENSP00000444095.1:p.Arg7Gly
ENST00000622132.4:c.19C>G ENSP00000478255.1:p.Arg7Gly
NM_000927.4:c.19C>G NP_000918.2:p.Arg7Gly
NM_001348944.1:c.19C>G NP_001335873.1:p.Arg7Gly
NM_001348945.1:c.229C>G NP_001335874.1:p.Arg77Gly
NM_001348946.1:c.19C>G NP_001335875.1:p.Arg7Gly
NM_001348946.2:c.19C>G MANE Select NP_001335875.1:p.Arg7Gly
NM_000927.5:c.19C>G NP_000918.2:p.Arg7Gly
NM_001348944.2:c.19C>G NP_001335873.1:p.Arg7Gly
NM_001348945.2:c.229C>G NP_001335874.1:p.Arg77Gly