Canonical Allele Identifier: CA4327982
Gene: ABCB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032583

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87531245A>G , CM000669.2:g.87531245A>G GRCh38
NC_000007.13:g.87160561A>G , CM000669.1:g.87160561A>G GRCh37
NC_000007.12:g.86998497A>G NCBI36
NG_011513.1:g.187004T>C

Transcript Alleles

HGVS Amino-acid change
NM_000927.4:c.2685+49T>C VV NP_000918.2:p.=
NM_001348944.1:c.2685+49T>C VV NP_001335873.1:p.=
NM_001348945.1:c.2895+49T>C VV NP_001335874.1:p.=
NM_001348946.1:c.2685+49T>C VV NP_001335875.1:p.=
ENST00000265724.7:c.2685+49T>C ENSP00000265724.3:p.=
ENST00000488737.6:n.327+49T>C
ENST00000496821.5:n.313+49T>C
ENST00000543898.5:c.2493+49T>C ENSP00000444095.1:p.=
ENST00000622132.4:c.2685+49T>C ENSP00000478255.1:p.=