Canonical Allele Identifier: CA1723626089
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515127T= , CM000669.2:g.87515127T= GRCh38
NC_000007.13:g.87144443T= , CM000669.1:g.87144443T= GRCh37
NC_000007.12:g.86982379T= NCBI36
NG_011513.1:g.203122A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3282+104A= ENSP00000265724.3:n.3282+104A=
ENST00000622132.5:c.3282+104A= MANE Select ENSP00000478255.1:n.3282+104A=
ENST00000265724.7:c.3282+104A= ENSP00000265724.3:n.3282+104A=
ENST00000475929.5:n.438+104A=
ENST00000488737.6:n.924+104A=
ENST00000543898.5:c.3090+104A= ENSP00000444095.1:n.3090+104A=
ENST00000622132.4:c.3282+104A= ENSP00000478255.1:n.3282+104A=
NM_000927.4:c.3282+104A= NP_000918.2:n.3282+104A=
NM_001348944.1:c.3282+104A= NP_001335873.1:n.3282+104A=
NM_001348945.1:c.3492+104A= NP_001335874.1:n.3492+104A=
NM_001348946.1:c.3282+104A= NP_001335875.1:n.3282+104A=
NM_001348946.2:c.3282+104A= MANE Select NP_001335875.1:n.3282+104A=
NM_000927.5:c.3282+104A= NP_000918.2:n.3282+104A=
NM_001348944.2:c.3282+104A= NP_001335873.1:n.3282+104A=
NM_001348945.2:c.3492+104A= NP_001335874.1:n.3492+104A=