Canonical Allele Identifier: CA1723646854
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1816717672

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87545139_87545141dup , CM000669.2:g.87545139_87545141dup GRCh38
NC_000007.13:g.87174455_87174457dup , CM000669.1:g.87174455_87174457dup GRCh37
NC_000007.12:g.87012391_87012393dup NCBI36
NG_011513.1:g.173112_173114dup

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.1888-138_1888-136dup ENSP00000265724.3:n.1888-138_1888-136dup
ENST00000622132.5:c.1888-138_1888-136dup MANE Select ENSP00000478255.1:n.1888-138_1888-136dup
ENST00000265724.7:c.1888-138_1888-136dup ENSP00000265724.3:n.1888-138_1888-136dup
ENST00000543898.5:c.1696-138_1696-136dup ENSP00000444095.1:n.1696-138_1696-136dup
ENST00000622132.4:c.1888-138_1888-136dup ENSP00000478255.1:n.1888-138_1888-136dup
NM_000927.4:c.1888-138_1888-136dup NP_000918.2:n.1888-138_1888-136dup
NM_001348944.1:c.1888-138_1888-136dup NP_001335873.1:n.1888-138_1888-136dup
NM_001348945.1:c.2098-138_2098-136dup NP_001335874.1:n.2098-138_2098-136dup
NM_001348946.1:c.1888-138_1888-136dup NP_001335875.1:n.1888-138_1888-136dup
NM_001348946.2:c.1888-138_1888-136dup MANE Select NP_001335875.1:n.1888-138_1888-136dup
NM_000927.5:c.1888-138_1888-136dup NP_000918.2:n.1888-138_1888-136dup
NM_001348944.2:c.1888-138_1888-136dup NP_001335873.1:n.1888-138_1888-136dup
NM_001348945.2:c.2098-138_2098-136dup NP_001335874.1:n.2098-138_2098-136dup