Canonical Allele Identifier: CA368062402

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87550026-G-A
• MyVariant Identifiers: chr7:g.87179342G>A (hg19) ; chr7:g.87550026G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550026G>A , CM000669.2:g.87550026G>A	GRCh38
NC_000007.13:g.87179342G>A , CM000669.1:g.87179342G>A	GRCh37
NC_000007.12:g.87017278G>A	NCBI36
NG_011513.1:g.168223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1379C>T	ENSP00000265724.3:p.Thr460Ile
ENST00000622132.5:c.1379C>T MANE Select	ENSP00000478255.1:p.Thr460Ile
ENST00000265724.7:c.1379C>T	ENSP00000265724.3:p.Thr460Ile
ENST00000482527.1:n.133C>T
ENST00000543898.5:c.1187C>T	ENSP00000444095.1:p.Thr396Ile
ENST00000622132.4:c.1379C>T	ENSP00000478255.1:p.Thr460Ile
NM_000927.4:c.1379C>T	NP_000918.2:p.Thr460Ile
NM_001348944.1:c.1379C>T	NP_001335873.1:p.Thr460Ile
NM_001348945.1:c.1589C>T	NP_001335874.1:p.Thr530Ile
NM_001348946.1:c.1379C>T	NP_001335875.1:p.Thr460Ile
NM_001348946.2:c.1379C>T MANE Select	NP_001335875.1:p.Thr460Ile
NM_000927.5:c.1379C>T	NP_000918.2:p.Thr460Ile
NM_001348944.2:c.1379C>T	NP_001335873.1:p.Thr460Ile
NM_001348945.2:c.1589C>T	NP_001335874.1:p.Thr530Ile