Canonical Allele Identifier: CA162118705

Gene: ABCB1

Linked Data

• dbSNP Id: rs28381919
• gnomAD v2: 7-87174460-ATGTGTGTCTG-A
• gnomAD v3: 7-87545144-ATGTGTGTCTG-A
• gnomAD v4: 7-87545144-ATGTGTGTCTG-A
• MyVariant Identifiers: chr7:g.87174461_87174470del (hg19) ; chr7:g.87545145_87545154del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545162_87545171del , CM000669.2:g.87545162_87545171del	GRCh38
NC_000007.13:g.87174478_87174487del , CM000669.1:g.87174478_87174487del	GRCh37
NC_000007.12:g.87012414_87012423del	NCBI36
NG_011513.1:g.173095_173104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1888-155_1888-146del	ENSP00000265724.3:n.1888-155_1888-146del
ENST00000622132.5:c.1888-155_1888-146del MANE Select	ENSP00000478255.1:n.1888-155_1888-146del
ENST00000265724.7:c.1888-155_1888-146del	ENSP00000265724.3:n.1888-155_1888-146del
ENST00000543898.5:c.1696-155_1696-146del	ENSP00000444095.1:n.1696-155_1696-146del
ENST00000622132.4:c.1888-155_1888-146del	ENSP00000478255.1:n.1888-155_1888-146del
NM_000927.4:c.1888-155_1888-146del	NP_000918.2:n.1888-155_1888-146del
NM_001348944.1:c.1888-155_1888-146del	NP_001335873.1:n.1888-155_1888-146del
NM_001348945.1:c.2098-155_2098-146del	NP_001335874.1:n.2098-155_2098-146del
NM_001348946.1:c.1888-155_1888-146del	NP_001335875.1:n.1888-155_1888-146del
NM_001348946.2:c.1888-155_1888-146del MANE Select	NP_001335875.1:n.1888-155_1888-146del
NM_000927.5:c.1888-155_1888-146del	NP_000918.2:n.1888-155_1888-146del
NM_001348944.2:c.1888-155_1888-146del	NP_001335873.1:n.1888-155_1888-146del
NM_001348945.2:c.2098-155_2098-146del	NP_001335874.1:n.2098-155_2098-146del