Canonical Allele Identifier: CA368054213

Gene: ABCB1

Linked Data

• dbSNP Id: rs2117129702
• COSMIC: COSM360322
• MyVariant Identifiers: chr7:g.87160614C>G (hg19) ; chr7:g.87531298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531298C>G , CM000669.2:g.87531298C>G	GRCh38
NC_000007.13:g.87160614C>G , CM000669.1:g.87160614C>G	GRCh37
NC_000007.12:g.86998550C>G	NCBI36
NG_011513.1:g.186951G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2681G>C	ENSP00000265724.3:p.Gly894Ala
ENST00000622132.5:c.2681G>C MANE Select	ENSP00000478255.1:p.Gly894Ala
ENST00000265724.7:c.2681G>C	ENSP00000265724.3:p.Gly894Ala
ENST00000488737.6:n.323G>C
ENST00000496821.5:n.309G>C
ENST00000543898.5:c.2489G>C	ENSP00000444095.1:p.Gly830Ala
ENST00000622132.4:c.2681G>C	ENSP00000478255.1:p.Gly894Ala
NM_000927.4:c.2681G>C	NP_000918.2:p.Gly894Ala
NM_001348944.1:c.2681G>C	NP_001335873.1:p.Gly894Ala
NM_001348945.1:c.2891G>C	NP_001335874.1:p.Gly964Ala
NM_001348946.1:c.2681G>C	NP_001335875.1:p.Gly894Ala
NM_001348946.2:c.2681G>C MANE Select	NP_001335875.1:p.Gly894Ala
NM_000927.5:c.2681G>C	NP_000918.2:p.Gly894Ala
NM_001348944.2:c.2681G>C	NP_001335873.1:p.Gly894Ala
NM_001348945.2:c.2891G>C	NP_001335874.1:p.Gly964Ala