Canonical Allele Identifier: CA843412145

Gene: ABCB1

Linked Data

• dbSNP Id: rs1446134074
• MyVariant Identifiers: chr7:g.87133209C>T (hg19) ; chr7:g.87503893C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503893C>T , CM000669.2:g.87503893C>T	GRCh38
NC_000007.13:g.87133209C>T , CM000669.1:g.87133209C>T	GRCh37
NC_000007.12:g.86971145C>T	NCBI36
NG_011513.1:g.214356G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.*350G>A	ENSP00000265724.3:n.*350G>A
ENST00000622132.5:c.*350G>A MANE Select	ENSP00000478255.1:n.*350G>A
ENST00000265724.7:c.*350G>A	ENSP00000265724.3:n.*350G>A
ENST00000488737.6:n.1835G>A
ENST00000543898.5:c.*350G>A	ENSP00000444095.1:n.*350G>A
ENST00000622132.4:c.*350G>A	ENSP00000478255.1:n.*350G>A
NM_000927.4:c.*350G>A	NP_000918.2:n.*350G>A
NM_001348944.1:c.*350G>A	NP_001335873.1:n.*350G>A
NM_001348945.1:c.*350G>A	NP_001335874.1:n.*350G>A
NM_001348946.1:c.*350G>A	NP_001335875.1:n.*350G>A
NM_001348946.2:c.*350G>A MANE Select	NP_001335875.1:n.*350G>A
NM_000927.5:c.*350G>A	NP_000918.2:n.*350G>A
NM_001348944.2:c.*350G>A	NP_001335873.1:n.*350G>A
NM_001348945.2:c.*350G>A	NP_001335874.1:n.*350G>A