Canonical Allele Identifier: CA1104133442

Gene: ABCB1

Linked Data

• dbSNP Id: rs1817074914
• gnomAD v3: 7-87551658-TTA-T
• gnomAD v4: 7-87551658-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87551659_87551660del , CM000669.2:g.87551659_87551660del	GRCh38
NC_000007.13:g.87180975_87180976del , CM000669.1:g.87180975_87180976del	GRCh37
NC_000007.12:g.87018911_87018912del	NCBI36
NG_011513.1:g.166589_166590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1000-822_1000-821del	ENSP00000265724.3:n.1000-822_1000-821del
ENST00000622132.5:c.1000-822_1000-821del MANE Select	ENSP00000478255.1:n.1000-822_1000-821del
ENST00000265724.7:c.1000-822_1000-821del	ENSP00000265724.3:n.1000-822_1000-821del
ENST00000543898.5:c.808-822_808-821del	ENSP00000444095.1:n.808-822_808-821del
ENST00000622132.4:c.1000-822_1000-821del	ENSP00000478255.1:n.1000-822_1000-821del
NM_000927.4:c.1000-822_1000-821del	NP_000918.2:n.1000-822_1000-821del
NM_001348944.1:c.1000-822_1000-821del	NP_001335873.1:n.1000-822_1000-821del
NM_001348945.1:c.1210-822_1210-821del	NP_001335874.1:n.1210-822_1210-821del
NM_001348946.1:c.1000-822_1000-821del	NP_001335875.1:n.1000-822_1000-821del
NM_001348946.2:c.1000-822_1000-821del MANE Select	NP_001335875.1:n.1000-822_1000-821del
NM_000927.5:c.1000-822_1000-821del	NP_000918.2:n.1000-822_1000-821del
NM_001348944.2:c.1000-822_1000-821del	NP_001335873.1:n.1000-822_1000-821del
NM_001348945.2:c.1210-822_1210-821del	NP_001335874.1:n.1210-822_1210-821del