Canonical Allele Identifier: CA456349827

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87516620-G-T
• MyVariant Identifiers: chr7:g.87145936G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516620G>T , CM000669.2:g.87516620G>T	GRCh38
NC_000007.13:g.87145936G>T , CM000669.1:g.87145936G>T	GRCh37
NC_000007.12:g.86983872G>T	NCBI36
NG_011513.1:g.201629C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2973C>A	ENSP00000265724.3:p.Val991=
ENST00000622132.5:c.2973C>A MANE Select	ENSP00000478255.1:p.Val991=
ENST00000265724.7:c.2973C>A	ENSP00000265724.3:p.Val991=
ENST00000475929.5:n.129C>A
ENST00000483831.1:n.531C>A
ENST00000488737.6:n.615C>A
ENST00000496821.5:n.601C>A
ENST00000543898.5:c.2781C>A	ENSP00000444095.1:p.Val927=
ENST00000622132.4:c.2973C>A	ENSP00000478255.1:p.Val991=
NM_000927.4:c.2973C>A	NP_000918.2:p.Val991=
NM_001348944.1:c.2973C>A	NP_001335873.1:p.Val991=
NM_001348945.1:c.3183C>A	NP_001335874.1:p.Val1061=
NM_001348946.1:c.2973C>A	NP_001335875.1:p.Val991=
NM_001348946.2:c.2973C>A MANE Select	NP_001335875.1:p.Val991=
NM_000927.5:c.2973C>A	NP_000918.2:p.Val991=
NM_001348944.2:c.2973C>A	NP_001335873.1:p.Val991=
NM_001348945.2:c.3183C>A	NP_001335874.1:p.Val1061=