Canonical Allele Identifier: CA16307104
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs2091766

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87545188C>T , CM000669.2:g.87545188C>T GRCh38
NC_000007.13:g.87174504C>T , CM000669.1:g.87174504C>T GRCh37
NC_000007.12:g.87012440C>T NCBI36
NG_011513.1:g.173061G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.1888-189G>A ENSP00000265724.3:p.=
ENST00000622132.5:c.1888-189G>A MANE Select ENSP00000478255.1:p.=
ENST00000265724.7:c.1888-189G>A ENSP00000265724.3:p.=
ENST00000543898.5:c.1696-189G>A ENSP00000444095.1:p.=
ENST00000622132.4:c.1888-189G>A ENSP00000478255.1:p.=
NM_000927.4:c.1888-189G>A NP_000918.2:p.=
NM_001348944.1:c.1888-189G>A NP_001335873.1:p.=
NM_001348945.1:c.2098-189G>A NP_001335874.1:p.=
NM_001348946.1:c.1888-189G>A NP_001335875.1:p.=
NM_001348946.2:c.1888-189G>A MANE Select NP_001335875.1:p.=
NM_000927.5:c.1888-189G>A NP_000918.2:p.=
NM_001348944.2:c.1888-189G>A NP_001335873.1:p.=
NM_001348945.2:c.2098-189G>A NP_001335874.1:p.=