Canonical Allele Identifier: CA1104120771

Gene: ABCB1

Linked Data

• dbSNP Id: rs1815272564
• gnomAD v3: 7-87516759-TG-T
• gnomAD v4: 7-87516759-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516763del , CM000669.2:g.87516763del	GRCh38
NC_000007.13:g.87146079del , CM000669.1:g.87146079del	GRCh37
NC_000007.12:g.86984015del	NCBI36
NG_011513.1:g.201489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2928-95del	ENSP00000265724.3:n.2928-95del
ENST00000622132.5:c.2928-95del MANE Select	ENSP00000478255.1:n.2928-95del
ENST00000265724.7:c.2928-95del	ENSP00000265724.3:n.2928-95del
ENST00000475929.5:n.84-95del
ENST00000483831.1:n.486-95del
ENST00000488737.6:n.570-95del
ENST00000496821.5:n.556-95del
ENST00000543898.5:c.2736-95del	ENSP00000444095.1:n.2736-95del
ENST00000622132.4:c.2928-95del	ENSP00000478255.1:n.2928-95del
NM_000927.4:c.2928-95del	NP_000918.2:n.2928-95del
NM_001348944.1:c.2928-95del	NP_001335873.1:n.2928-95del
NM_001348945.1:c.3138-95del	NP_001335874.1:n.3138-95del
NM_001348946.1:c.2928-95del	NP_001335875.1:n.2928-95del
NM_001348946.2:c.2928-95del MANE Select	NP_001335875.1:n.2928-95del
NM_000927.5:c.2928-95del	NP_000918.2:n.2928-95del
NM_001348944.2:c.2928-95del	NP_001335873.1:n.2928-95del
NM_001348945.2:c.3138-95del	NP_001335874.1:n.3138-95del