Canonical Allele Identifier: CA368050295

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87150169G>C (hg19) ; chr7:g.87520853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520853G>C , CM000669.2:g.87520853G>C	GRCh38
NC_000007.13:g.87150169G>C , CM000669.1:g.87150169G>C	GRCh37
NC_000007.12:g.86988105G>C	NCBI36
NG_011513.1:g.197396C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2709C>G	ENSP00000265724.3:p.Asn903Lys
ENST00000622132.5:c.2709C>G MANE Select	ENSP00000478255.1:p.Asn903Lys
ENST00000265724.7:c.2709C>G	ENSP00000265724.3:p.Asn903Lys
ENST00000483831.1:n.267C>G
ENST00000488737.6:n.351C>G
ENST00000496821.5:n.337C>G
ENST00000543898.5:c.2517C>G	ENSP00000444095.1:p.Asn839Lys
ENST00000622132.4:c.2709C>G	ENSP00000478255.1:p.Asn903Lys
NM_000927.4:c.2709C>G	NP_000918.2:p.Asn903Lys
NM_001348944.1:c.2709C>G	NP_001335873.1:p.Asn903Lys
NM_001348945.1:c.2919C>G	NP_001335874.1:p.Asn973Lys
NM_001348946.1:c.2709C>G	NP_001335875.1:p.Asn903Lys
NM_001348946.2:c.2709C>G MANE Select	NP_001335875.1:p.Asn903Lys
NM_000927.5:c.2709C>G	NP_000918.2:p.Asn903Lys
NM_001348944.2:c.2709C>G	NP_001335873.1:p.Asn903Lys
NM_001348945.2:c.2919C>G	NP_001335874.1:p.Asn973Lys