Canonical Allele Identifier: CA368043674

Gene: ABCB1

Linked Data

• dbSNP Id: rs200192869
• MyVariant Identifiers: chr7:g.87144597T>C (hg19) ; chr7:g.87515281T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515281T>C , CM000669.2:g.87515281T>C	GRCh38
NC_000007.13:g.87144597T>C , CM000669.1:g.87144597T>C	GRCh37
NC_000007.12:g.86982533T>C	NCBI36
NG_011513.1:g.202968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3232A>G	ENSP00000265724.3:p.Thr1078Ala
ENST00000622132.5:c.3232A>G MANE Select	ENSP00000478255.1:p.Thr1078Ala
ENST00000265724.7:c.3232A>G	ENSP00000265724.3:p.Thr1078Ala
ENST00000475929.5:n.388A>G
ENST00000488737.6:n.874A>G
ENST00000496821.5:n.860A>G
ENST00000543898.5:c.3040A>G	ENSP00000444095.1:p.Thr1014Ala
ENST00000622132.4:c.3232A>G	ENSP00000478255.1:p.Thr1078Ala
NM_000927.4:c.3232A>G	NP_000918.2:p.Thr1078Ala
NM_001348944.1:c.3232A>G	NP_001335873.1:p.Thr1078Ala
NM_001348945.1:c.3442A>G	NP_001335874.1:p.Thr1148Ala
NM_001348946.1:c.3232A>G	NP_001335875.1:p.Thr1078Ala
NM_001348946.2:c.3232A>G MANE Select	NP_001335875.1:p.Thr1078Ala
NM_000927.5:c.3232A>G	NP_000918.2:p.Thr1078Ala
NM_001348944.2:c.3232A>G	NP_001335873.1:p.Thr1078Ala
NM_001348945.2:c.3442A>G	NP_001335874.1:p.Thr1148Ala