Canonical Allele Identifier: CA1723648224
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87566224T= , CM000669.2:g.87566224T= GRCh38
NC_000007.13:g.87195540T= , CM000669.1:g.87195540T= GRCh37
NC_000007.12:g.87033476T= NCBI36
NG_011513.1:g.152025A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.548A= ENSP00000265724.3:p.Asn183=
ENST00000622132.5:c.548A= MANE Select ENSP00000478255.1:p.Asn183=
ENST00000265724.7:c.548A= ENSP00000265724.3:p.Asn183=
ENST00000543898.5:c.356A= ENSP00000444095.1:p.Asn119=
ENST00000622132.4:c.548A= ENSP00000478255.1:p.Asn183=
NM_000927.4:c.548A= NP_000918.2:p.Asn183=
NM_001348944.1:c.548A= NP_001335873.1:p.Asn183=
NM_001348945.1:c.758A= NP_001335874.1:p.Asn253=
NM_001348946.1:c.548A= NP_001335875.1:p.Asn183=
NM_001348946.2:c.548A= MANE Select NP_001335875.1:p.Asn183=
NM_000927.5:c.548A= NP_000918.2:p.Asn183=
NM_001348944.2:c.548A= NP_001335873.1:p.Asn183=
NM_001348945.2:c.758A= NP_001335874.1:p.Asn253=