Canonical Allele Identifier: CA162101657

Gene: ABCB1

Linked Data

• dbSNP Id: rs756182063
• gnomAD v2: 7-87144879-ATTTAT-A
• gnomAD v3: 7-87515563-ATTTAT-A
• gnomAD v4: 7-87515563-ATTTAT-A
• MyVariant Identifiers: chr7:g.87144880_87144884del (hg19) ; chr7:g.87515564_87515568del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515573_87515577del , CM000669.2:g.87515573_87515577del	GRCh38
NC_000007.13:g.87144889_87144893del , CM000669.1:g.87144889_87144893del	GRCh37
NC_000007.12:g.86982825_86982829del	NCBI36
NG_011513.1:g.202681_202685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3085-140_3085-136del	ENSP00000265724.3:n.3085-140_3085-136del
ENST00000622132.5:c.3085-140_3085-136del MANE Select	ENSP00000478255.1:n.3085-140_3085-136del
ENST00000265724.7:c.3085-140_3085-136del	ENSP00000265724.3:n.3085-140_3085-136del
ENST00000475929.5:n.241-140_241-136del
ENST00000488737.6:n.727-140_727-136del
ENST00000496821.5:n.713-140_713-136del
ENST00000543898.5:c.2893-140_2893-136del	ENSP00000444095.1:n.2893-140_2893-136del
ENST00000622132.4:c.3085-140_3085-136del	ENSP00000478255.1:n.3085-140_3085-136del
NM_000927.4:c.3085-140_3085-136del	NP_000918.2:n.3085-140_3085-136del
NM_001348944.1:c.3085-140_3085-136del	NP_001335873.1:n.3085-140_3085-136del
NM_001348945.1:c.3295-140_3295-136del	NP_001335874.1:n.3295-140_3295-136del
NM_001348946.1:c.3085-140_3085-136del	NP_001335875.1:n.3085-140_3085-136del
NM_001348946.2:c.3085-140_3085-136del MANE Select	NP_001335875.1:n.3085-140_3085-136del
NM_000927.5:c.3085-140_3085-136del	NP_000918.2:n.3085-140_3085-136del
NM_001348944.2:c.3085-140_3085-136del	NP_001335873.1:n.3085-140_3085-136del
NM_001348945.2:c.3295-140_3295-136del	NP_001335874.1:n.3295-140_3295-136del