Canonical Allele Identifier: CA843419100

Gene: ABCB1

Linked Data

• dbSNP Id: rs1449846064
• gnomAD v3: 7-87520413-GCAC-G
• gnomAD v4: 7-87520413-GCAC-G
• MyVariant Identifiers: chr7:g.87149730_87149732del (hg19) ; chr7:g.87520414_87520416del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520416_87520418del , CM000669.2:g.87520416_87520418del	GRCh38
NC_000007.13:g.87149732_87149734del , CM000669.1:g.87149732_87149734del	GRCh37
NC_000007.12:g.86987668_86987670del	NCBI36
NG_011513.1:g.197833_197835del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2786+360_2786+362del	ENSP00000265724.3:n.2786+360_2786+362del
ENST00000622132.5:c.2786+360_2786+362del MANE Select	ENSP00000478255.1:n.2786+360_2786+362del
ENST00000265724.7:c.2786+360_2786+362del	ENSP00000265724.3:n.2786+360_2786+362del
ENST00000483831.1:n.344+360_344+362del
ENST00000488737.6:n.428+360_428+362del
ENST00000496821.5:n.414+360_414+362del
ENST00000543898.5:c.2594+360_2594+362del	ENSP00000444095.1:n.2594+360_2594+362del
ENST00000622132.4:c.2786+360_2786+362del	ENSP00000478255.1:n.2786+360_2786+362del
NM_000927.4:c.2786+360_2786+362del	NP_000918.2:n.2786+360_2786+362del
NM_001348944.1:c.2786+360_2786+362del	NP_001335873.1:n.2786+360_2786+362del
NM_001348945.1:c.2996+360_2996+362del	NP_001335874.1:n.2996+360_2996+362del
NM_001348946.1:c.2786+360_2786+362del	NP_001335875.1:n.2786+360_2786+362del
NM_001348946.2:c.2786+360_2786+362del MANE Select	NP_001335875.1:n.2786+360_2786+362del
NM_000927.5:c.2786+360_2786+362del	NP_000918.2:n.2786+360_2786+362del
NM_001348944.2:c.2786+360_2786+362del	NP_001335873.1:n.2786+360_2786+362del
NM_001348945.2:c.2996+360_2996+362del	NP_001335874.1:n.2996+360_2996+362del