Canonical Allele Identifier: CA843419070

Gene: ABCB1

Linked Data

• dbSNP Id: rs1240997021
• MyVariant Identifiers: chr7:g.87149651A>C (hg19) ; chr7:g.87520335A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520335A>C , CM000669.2:g.87520335A>C	GRCh38
NC_000007.13:g.87149651A>C , CM000669.1:g.87149651A>C	GRCh37
NC_000007.12:g.86987587A>C	NCBI36
NG_011513.1:g.197914T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2786+441T>G	ENSP00000265724.3:n.2786+441T>G
ENST00000622132.5:c.2786+441T>G MANE Select	ENSP00000478255.1:n.2786+441T>G
ENST00000265724.7:c.2786+441T>G	ENSP00000265724.3:n.2786+441T>G
ENST00000483831.1:n.344+441T>G
ENST00000488737.6:n.428+441T>G
ENST00000496821.5:n.414+441T>G
ENST00000543898.5:c.2594+441T>G	ENSP00000444095.1:n.2594+441T>G
ENST00000622132.4:c.2786+441T>G	ENSP00000478255.1:n.2786+441T>G
NM_000927.4:c.2786+441T>G	NP_000918.2:n.2786+441T>G
NM_001348944.1:c.2786+441T>G	NP_001335873.1:n.2786+441T>G
NM_001348945.1:c.2996+441T>G	NP_001335874.1:n.2996+441T>G
NM_001348946.1:c.2786+441T>G	NP_001335875.1:n.2786+441T>G
NM_001348946.2:c.2786+441T>G MANE Select	NP_001335875.1:n.2786+441T>G
NM_000927.5:c.2786+441T>G	NP_000918.2:n.2786+441T>G
NM_001348944.2:c.2786+441T>G	NP_001335873.1:n.2786+441T>G
NM_001348945.2:c.2996+441T>G	NP_001335874.1:n.2996+441T>G