Canonical Allele Identifier: CA162474292

Gene: ABCB1

Linked Data

• dbSNP Id: rs201808019
• gnomAD v3: 7-87600894-C-T
• gnomAD v4: 7-87600894-C-T
• MyVariant Identifiers: chr7:g.87230210C>T (hg19) ; chr7:g.87600894C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600894C>T , CM000669.2:g.87600894C>T	GRCh38
NC_000007.13:g.87230210C>T , CM000669.1:g.87230210C>T	GRCh37
NC_000007.12:g.87068146C>T	NCBI36
NG_011513.1:g.117355G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.-146G>A	ENSP00000265724.3:n.-146G>A
ENST00000265724.7:c.-146G>A	ENSP00000265724.3:n.-146G>A
ENST00000416177.1:c.-77-69G>A	ENSP00000399419.1:n.-77-69G>A
ENST00000476862.1:n.501G>A
ENST00000543898.5:c.-146G>A	ENSP00000444095.1:n.-146G>A
ENST00000622132.4:c.-146G>A	ENSP00000478255.1:n.-146G>A
NM_000927.4:c.-146G>A	NP_000918.2:n.-146G>A
NM_001348944.1:c.-77-69G>A	NP_001335873.1:n.-77-69G>A
NM_001348945.1:c.134-69G>A	NP_001335874.1:n.134-69G>A
NM_000927.5:c.-146G>A	NP_000918.2:n.-146G>A
NM_001348944.2:c.-77-69G>A	NP_001335873.1:n.-77-69G>A
NM_001348945.2:c.134-69G>A	NP_001335874.1:n.134-69G>A