Canonical Allele Identifier: CA1104131666

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816696542
• gnomAD v3: 7-87544763-CA-C
• gnomAD v4: 7-87544763-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87544764del , CM000669.2:g.87544764del	GRCh38
NC_000007.13:g.87174080del , CM000669.1:g.87174080del	GRCh37
NC_000007.12:g.87012016del	NCBI36
NG_011513.1:g.173485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2064+59del	ENSP00000265724.3:n.2064+59del
ENST00000622132.5:c.2064+59del MANE Select	ENSP00000478255.1:n.2064+59del
ENST00000265724.7:c.2064+59del	ENSP00000265724.3:n.2064+59del
ENST00000543898.5:c.1872+59del	ENSP00000444095.1:n.1872+59del
ENST00000622132.4:c.2064+59del	ENSP00000478255.1:n.2064+59del
NM_000927.4:c.2064+59del	NP_000918.2:n.2064+59del
NM_001348944.1:c.2064+59del	NP_001335873.1:n.2064+59del
NM_001348945.1:c.2274+59del	NP_001335874.1:n.2274+59del
NM_001348946.1:c.2064+59del	NP_001335875.1:n.2064+59del
NM_001348946.2:c.2064+59del MANE Select	NP_001335875.1:n.2064+59del
NM_000927.5:c.2064+59del	NP_000918.2:n.2064+59del
NM_001348944.2:c.2064+59del	NP_001335873.1:n.2064+59del
NM_001348945.2:c.2274+59del	NP_001335874.1:n.2274+59del