Canonical Allele Identifier: CA368062533

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179511C>G (hg19) ; chr7:g.87550195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550195C>G , CM000669.2:g.87550195C>G	GRCh38
NC_000007.13:g.87179511C>G , CM000669.1:g.87179511C>G	GRCh37
NC_000007.12:g.87017447C>G	NCBI36
NG_011513.1:g.168054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1326G>C	ENSP00000265724.3:p.Arg442Ser
ENST00000622132.5:c.1326G>C MANE Select	ENSP00000478255.1:p.Arg442Ser
ENST00000265724.7:c.1326G>C	ENSP00000265724.3:p.Arg442Ser
ENST00000543898.5:c.1134G>C	ENSP00000444095.1:p.Arg378Ser
ENST00000622132.4:c.1326G>C	ENSP00000478255.1:p.Arg442Ser
NM_000927.4:c.1326G>C	NP_000918.2:p.Arg442Ser
NM_001348944.1:c.1326G>C	NP_001335873.1:p.Arg442Ser
NM_001348945.1:c.1536G>C	NP_001335874.1:p.Arg512Ser
NM_001348946.1:c.1326G>C	NP_001335875.1:p.Arg442Ser
NM_001348946.2:c.1326G>C MANE Select	NP_001335875.1:p.Arg442Ser
NM_000927.5:c.1326G>C	NP_000918.2:p.Arg442Ser
NM_001348944.2:c.1326G>C	NP_001335873.1:p.Arg442Ser
NM_001348945.2:c.1536G>C	NP_001335874.1:p.Arg512Ser