Canonical Allele Identifier: CA1723646889

Gene: ABCB1

Linked Data

• dbSNP Id: rs1042567834

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545167_87545176del , CM000669.2:g.87545167_87545176del	GRCh38
NC_000007.13:g.87174483_87174492del , CM000669.1:g.87174483_87174492del	GRCh37
NC_000007.12:g.87012419_87012428del	NCBI36
NG_011513.1:g.173077_173086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1888-173_1888-164del	ENSP00000265724.3:n.1888-173_1888-164del
ENST00000622132.5:c.1888-173_1888-164del MANE Select	ENSP00000478255.1:n.1888-173_1888-164del
ENST00000265724.7:c.1888-173_1888-164del	ENSP00000265724.3:n.1888-173_1888-164del
ENST00000543898.5:c.1696-173_1696-164del	ENSP00000444095.1:n.1696-173_1696-164del
ENST00000622132.4:c.1888-173_1888-164del	ENSP00000478255.1:n.1888-173_1888-164del
NM_000927.4:c.1888-173_1888-164del	NP_000918.2:n.1888-173_1888-164del
NM_001348944.1:c.1888-173_1888-164del	NP_001335873.1:n.1888-173_1888-164del
NM_001348945.1:c.2098-173_2098-164del	NP_001335874.1:n.2098-173_2098-164del
NM_001348946.1:c.1888-173_1888-164del	NP_001335875.1:n.1888-173_1888-164del
NM_001348946.2:c.1888-173_1888-164del MANE Select	NP_001335875.1:n.1888-173_1888-164del
NM_000927.5:c.1888-173_1888-164del	NP_000918.2:n.1888-173_1888-164del
NM_001348944.2:c.1888-173_1888-164del	NP_001335873.1:n.1888-173_1888-164del
NM_001348945.2:c.2098-173_2098-164del	NP_001335874.1:n.2098-173_2098-164del