Canonical Allele Identifier: CA1723628760

Gene: ABCB1

Linked Data

• dbSNP Id: rs1815483954
• gnomAD v4: 7-87521062-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87521062A>T , CM000669.2:g.87521062A>T	GRCh38
NC_000007.13:g.87150378A>T , CM000669.1:g.87150378A>T	GRCh37
NC_000007.12:g.86988314A>T	NCBI36
NG_011513.1:g.197187T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2686-186T>A	ENSP00000265724.3:n.2686-186T>A
ENST00000622132.5:c.2686-186T>A MANE Select	ENSP00000478255.1:n.2686-186T>A
ENST00000265724.7:c.2686-186T>A	ENSP00000265724.3:n.2686-186T>A
ENST00000483831.1:n.58T>A
ENST00000488737.6:n.328-186T>A
ENST00000496821.5:n.314-186T>A
ENST00000543898.5:c.2494-186T>A	ENSP00000444095.1:n.2494-186T>A
ENST00000622132.4:c.2686-186T>A	ENSP00000478255.1:n.2686-186T>A
NM_000927.4:c.2686-186T>A	NP_000918.2:n.2686-186T>A
NM_001348944.1:c.2686-186T>A	NP_001335873.1:n.2686-186T>A
NM_001348945.1:c.2896-186T>A	NP_001335874.1:n.2896-186T>A
NM_001348946.1:c.2686-186T>A	NP_001335875.1:n.2686-186T>A
NM_001348946.2:c.2686-186T>A MANE Select	NP_001335875.1:n.2686-186T>A
NM_000927.5:c.2686-186T>A	NP_000918.2:n.2686-186T>A
NM_001348944.2:c.2686-186T>A	NP_001335873.1:n.2686-186T>A
NM_001348945.2:c.2896-186T>A	NP_001335874.1:n.2896-186T>A