Canonical Allele Identifier: CA456351467

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150145A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520829A>G , CM000669.2:g.87520829A>G	GRCh38
NC_000007.13:g.87150145A>G , CM000669.1:g.87150145A>G	GRCh37
NC_000007.12:g.86988081A>G	NCBI36
NG_011513.1:g.197420T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2733T>C	ENSP00000265724.3:p.Thr911=
ENST00000622132.5:c.2733T>C MANE Select	ENSP00000478255.1:p.Thr911=
ENST00000265724.7:c.2733T>C	ENSP00000265724.3:p.Thr911=
ENST00000483831.1:n.291T>C
ENST00000488737.6:n.375T>C
ENST00000496821.5:n.361T>C
ENST00000543898.5:c.2541T>C	ENSP00000444095.1:p.Thr847=
ENST00000622132.4:c.2733T>C	ENSP00000478255.1:p.Thr911=
NM_000927.4:c.2733T>C	NP_000918.2:p.Thr911=
NM_001348944.1:c.2733T>C	NP_001335873.1:p.Thr911=
NM_001348945.1:c.2943T>C	NP_001335874.1:p.Thr981=
NM_001348946.1:c.2733T>C	NP_001335875.1:p.Thr911=
NM_001348946.2:c.2733T>C MANE Select	NP_001335875.1:p.Thr911=
NM_000927.5:c.2733T>C	NP_000918.2:p.Thr911=
NM_001348944.2:c.2733T>C	NP_001335873.1:p.Thr911=
NM_001348945.2:c.2943T>C	NP_001335874.1:p.Thr981=