Canonical Allele Identifier: CA368049945

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150099G>T (hg19) ; chr7:g.87520783G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520783G>T , CM000669.2:g.87520783G>T	GRCh38
NC_000007.13:g.87150099G>T , CM000669.1:g.87150099G>T	GRCh37
NC_000007.12:g.86988035G>T	NCBI36
NG_011513.1:g.197466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2779C>A	ENSP00000265724.3:p.Pro927Thr
ENST00000622132.5:c.2779C>A MANE Select	ENSP00000478255.1:p.Pro927Thr
ENST00000265724.7:c.2779C>A	ENSP00000265724.3:p.Pro927Thr
ENST00000483831.1:n.337C>A
ENST00000488737.6:n.421C>A
ENST00000496821.5:n.407C>A
ENST00000543898.5:c.2587C>A	ENSP00000444095.1:p.Pro863Thr
ENST00000622132.4:c.2779C>A	ENSP00000478255.1:p.Pro927Thr
NM_000927.4:c.2779C>A	NP_000918.2:p.Pro927Thr
NM_001348944.1:c.2779C>A	NP_001335873.1:p.Pro927Thr
NM_001348945.1:c.2989C>A	NP_001335874.1:p.Pro997Thr
NM_001348946.1:c.2779C>A	NP_001335875.1:p.Pro927Thr
NM_001348946.2:c.2779C>A MANE Select	NP_001335875.1:p.Pro927Thr
NM_000927.5:c.2779C>A	NP_000918.2:p.Pro927Thr
NM_001348944.2:c.2779C>A	NP_001335873.1:p.Pro927Thr
NM_001348945.2:c.2989C>A	NP_001335874.1:p.Pro997Thr