Canonical Allele Identifier: CA1723631302

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816013443

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530841_87530846dup , CM000669.2:g.87530841_87530846dup	GRCh38
NC_000007.13:g.87160157_87160162dup , CM000669.1:g.87160157_87160162dup	GRCh37
NC_000007.12:g.86998093_86998098dup	NCBI36
NG_011513.1:g.187404_187409dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+449_2685+454dup	ENSP00000265724.3:n.2685+449_2685+454dup
ENST00000622132.5:c.2685+449_2685+454dup MANE Select	ENSP00000478255.1:n.2685+449_2685+454dup
ENST00000265724.7:c.2685+449_2685+454dup	ENSP00000265724.3:n.2685+449_2685+454dup
ENST00000488737.6:n.327+449_327+454dup
ENST00000496821.5:n.313+449_313+454dup
ENST00000543898.5:c.2493+449_2493+454dup	ENSP00000444095.1:n.2493+449_2493+454dup
ENST00000622132.4:c.2685+449_2685+454dup	ENSP00000478255.1:n.2685+449_2685+454dup
NM_000927.4:c.2685+449_2685+454dup	NP_000918.2:n.2685+449_2685+454dup
NM_001348944.1:c.2685+449_2685+454dup	NP_001335873.1:n.2685+449_2685+454dup
NM_001348945.1:c.2895+449_2895+454dup	NP_001335874.1:n.2895+449_2895+454dup
NM_001348946.1:c.2685+449_2685+454dup	NP_001335875.1:n.2685+449_2685+454dup
NM_001348946.2:c.2685+449_2685+454dup MANE Select	NP_001335875.1:n.2685+449_2685+454dup
NM_000927.5:c.2685+449_2685+454dup	NP_000918.2:n.2685+449_2685+454dup
NM_001348944.2:c.2685+449_2685+454dup	NP_001335873.1:n.2685+449_2685+454dup
NM_001348945.2:c.2895+449_2895+454dup	NP_001335874.1:n.2895+449_2895+454dup