Canonical Allele Identifier: CA1723651567
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87550249G= , CM000669.2:g.87550249G= GRCh38
NC_000007.13:g.87179565G= , CM000669.1:g.87179565G= GRCh37
NC_000007.12:g.87017501G= NCBI36
NG_011513.1:g.168000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1272C= ENSP00000265724.3:p.Ala424=
ENST00000622132.5:c.1272C= MANE Select ENSP00000478255.1:p.Ala424=
ENST00000265724.7:c.1272C= ENSP00000265724.3:p.Ala424=
ENST00000543898.5:c.1080C= ENSP00000444095.1:p.Ala360=
ENST00000622132.4:c.1272C= ENSP00000478255.1:p.Ala424=
NM_000927.4:c.1272C= NP_000918.2:p.Ala424=
NM_001348944.1:c.1272C= NP_001335873.1:p.Ala424=
NM_001348945.1:c.1482C= NP_001335874.1:p.Ala494=
NM_001348946.1:c.1272C= NP_001335875.1:p.Ala424=
NM_001348946.2:c.1272C= MANE Select NP_001335875.1:p.Ala424=
NM_000927.5:c.1272C= NP_000918.2:p.Ala424=
NM_001348944.2:c.1272C= NP_001335873.1:p.Ala424=
NM_001348945.2:c.1482C= NP_001335874.1:p.Ala494=