Canonical Allele Identifier: CA1104132785

Gene: ABCB1

Linked Data

• dbSNP Id: rs1815212124
• gnomAD v3: 7-87515720-A-T
• gnomAD v4: 7-87515720-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515720A>T , CM000669.2:g.87515720A>T	GRCh38
NC_000007.13:g.87145036A>T , CM000669.1:g.87145036A>T	GRCh37
NC_000007.12:g.86982972A>T	NCBI36
NG_011513.1:g.202529T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3085-292T>A	ENSP00000265724.3:n.3085-292T>A
ENST00000622132.5:c.3085-292T>A MANE Select	ENSP00000478255.1:n.3085-292T>A
ENST00000265724.7:c.3085-292T>A	ENSP00000265724.3:n.3085-292T>A
ENST00000475929.5:n.241-292T>A
ENST00000488737.6:n.727-292T>A
ENST00000496821.5:n.713-292T>A
ENST00000543898.5:c.2893-292T>A	ENSP00000444095.1:n.2893-292T>A
ENST00000622132.4:c.3085-292T>A	ENSP00000478255.1:n.3085-292T>A
NM_000927.4:c.3085-292T>A	NP_000918.2:n.3085-292T>A
NM_001348944.1:c.3085-292T>A	NP_001335873.1:n.3085-292T>A
NM_001348945.1:c.3295-292T>A	NP_001335874.1:n.3295-292T>A
NM_001348946.1:c.3085-292T>A	NP_001335875.1:n.3085-292T>A
NM_001348946.2:c.3085-292T>A MANE Select	NP_001335875.1:n.3085-292T>A
NM_000927.5:c.3085-292T>A	NP_000918.2:n.3085-292T>A
NM_001348944.2:c.3085-292T>A	NP_001335873.1:n.3085-292T>A
NM_001348945.2:c.3295-292T>A	NP_001335874.1:n.3295-292T>A