Canonical Allele Identifier: CA162101605
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs200256019

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515400C>T , CM000669.2:g.87515400C>T GRCh38
NC_000007.13:g.87144716C>T , CM000669.1:g.87144716C>T GRCh37
NC_000007.12:g.86982652C>T NCBI36
NG_011513.1:g.202849G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3113G>A ENSP00000265724.3:p.Gly1038Asp
ENST00000622132.5:c.3113G>A MANE Select ENSP00000478255.1:p.Gly1038Asp
ENST00000265724.7:c.3113G>A ENSP00000265724.3:p.Gly1038Asp
ENST00000475929.5:n.269G>A
ENST00000488737.6:n.755G>A
ENST00000496821.5:n.741G>A
ENST00000543898.5:c.2921G>A ENSP00000444095.1:p.Gly974Asp
ENST00000622132.4:c.3113G>A ENSP00000478255.1:p.Gly1038Asp
NM_000927.4:c.3113G>A NP_000918.2:p.Gly1038Asp
NM_001348944.1:c.3113G>A NP_001335873.1:p.Gly1038Asp
NM_001348945.1:c.3323G>A NP_001335874.1:p.Gly1108Asp
NM_001348946.1:c.3113G>A NP_001335875.1:p.Gly1038Asp
NM_001348946.2:c.3113G>A MANE Select NP_001335875.1:p.Gly1038Asp
NM_000927.5:c.3113G>A NP_000918.2:p.Gly1038Asp
NM_001348944.2:c.3113G>A NP_001335873.1:p.Gly1038Asp
NM_001348945.2:c.3323G>A NP_001335874.1:p.Gly1108Asp