Canonical Allele Identifier: CA1723623725
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87509343A= , CM000669.2:g.87509343A= GRCh38
NC_000007.13:g.87138659A= , CM000669.1:g.87138659A= GRCh37
NC_000007.12:g.86976595A= NCBI36
NG_011513.1:g.208906T=

Transcript Alleles

HGVS Amino-acid Change
NM_001348946.2:c.3421T= MANE Select NP_001335875.1:p.Ser1141=
ENST00000622132.5:c.3421T= MANE Select ENSP00000478255.1:p.Ser1141=
NM_000927.4:c.3421T= NP_000918.2:p.Ser1141=
NM_000927.5:c.3421T= NP_000918.2:p.Ser1141=
NM_001348944.1:c.3421T= NP_001335873.1:p.Ser1141=
NM_001348944.2:c.3421T= NP_001335873.1:p.Ser1141=
NM_001348945.1:c.3631T= NP_001335874.1:p.Ser1211=
NM_001348945.2:c.3631T= NP_001335874.1:p.Ser1211=
NM_001348946.1:c.3421T= NP_001335875.1:p.Ser1141=
ENST00000265724.7:c.3421T= ENSP00000265724.3:p.Ser1141=
ENST00000265724.8:c.3421T= ENSP00000265724.3:p.Ser1141=
ENST00000475929.5:n.577T=
ENST00000488737.6:n.1063T=
ENST00000543898.5:c.3229T= ENSP00000444095.1:p.Ser1077=
ENST00000622132.4:c.3421T= ENSP00000478255.1:p.Ser1141=