Canonical Allele Identifier: CA575862182

Gene: ABCB1

Linked Data

• dbSNP Id: rs1489259826
• gnomAD v2: 7-87165896-TTA-T
• gnomAD v4: 7-87536580-TTA-T
• MyVariant Identifiers: chr7:g.87165897_87165898del (hg19) ; chr7:g.87536581_87536582del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87536582_87536583del , CM000669.2:g.87536582_87536583del	GRCh38
NC_000007.13:g.87165898_87165899del , CM000669.1:g.87165898_87165899del	GRCh37
NC_000007.12:g.87003834_87003835del	NCBI36
NG_011513.1:g.181667_181668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2398-41_2398-40del	ENSP00000265724.3:n.2398-41_2398-40del
ENST00000622132.5:c.2398-41_2398-40del MANE Select	ENSP00000478255.1:n.2398-41_2398-40del
ENST00000265724.7:c.2398-41_2398-40del	ENSP00000265724.3:n.2398-41_2398-40del
ENST00000496821.5:n.26-41_26-40del
ENST00000543898.5:c.2206-41_2206-40del	ENSP00000444095.1:n.2206-41_2206-40del
ENST00000622132.4:c.2398-41_2398-40del	ENSP00000478255.1:n.2398-41_2398-40del
NM_000927.4:c.2398-41_2398-40del	NP_000918.2:n.2398-41_2398-40del
NM_001348944.1:c.2398-41_2398-40del	NP_001335873.1:n.2398-41_2398-40del
NM_001348945.1:c.2608-41_2608-40del	NP_001335874.1:n.2608-41_2608-40del
NM_001348946.1:c.2398-41_2398-40del	NP_001335875.1:n.2398-41_2398-40del
NM_001348946.2:c.2398-41_2398-40del MANE Select	NP_001335875.1:n.2398-41_2398-40del
NM_000927.5:c.2398-41_2398-40del	NP_000918.2:n.2398-41_2398-40del
NM_001348944.2:c.2398-41_2398-40del	NP_001335873.1:n.2398-41_2398-40del
NM_001348945.2:c.2608-41_2608-40del	NP_001335874.1:n.2608-41_2608-40del