Canonical Allele Identifier: CA368054253

Gene: ABCB1

Linked Data

• dbSNP Id: rs2117129803
• MyVariant Identifiers: chr7:g.87160620C>G (hg19) ; chr7:g.87531304C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531304C>G , CM000669.2:g.87531304C>G	GRCh38
NC_000007.13:g.87160620C>G , CM000669.1:g.87160620C>G	GRCh37
NC_000007.12:g.86998556C>G	NCBI36
NG_011513.1:g.186945G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2675G>C	ENSP00000265724.3:p.Gly892Ala
ENST00000622132.5:c.2675G>C MANE Select	ENSP00000478255.1:p.Gly892Ala
ENST00000265724.7:c.2675G>C	ENSP00000265724.3:p.Gly892Ala
ENST00000488737.6:n.317G>C
ENST00000496821.5:n.303G>C
ENST00000543898.5:c.2483G>C	ENSP00000444095.1:p.Gly828Ala
ENST00000622132.4:c.2675G>C	ENSP00000478255.1:p.Gly892Ala
NM_000927.4:c.2675G>C	NP_000918.2:p.Gly892Ala
NM_001348944.1:c.2675G>C	NP_001335873.1:p.Gly892Ala
NM_001348945.1:c.2885G>C	NP_001335874.1:p.Gly962Ala
NM_001348946.1:c.2675G>C	NP_001335875.1:p.Gly892Ala
NM_001348946.2:c.2675G>C MANE Select	NP_001335875.1:p.Gly892Ala
NM_000927.5:c.2675G>C	NP_000918.2:p.Gly892Ala
NM_001348944.2:c.2675G>C	NP_001335873.1:p.Gly892Ala
NM_001348945.2:c.2885G>C	NP_001335874.1:p.Gly962Ala