Canonical Allele Identifier: CA162098621

Gene: ABCB1

Linked Data

• dbSNP Id: rs200185314
• gnomAD v4: 7-87503886-A-G
• MyVariant Identifiers: chr7:g.87133202A>G (hg19) ; chr7:g.87503886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503886A>G , CM000669.2:g.87503886A>G	GRCh38
NC_000007.13:g.87133202A>G , CM000669.1:g.87133202A>G	GRCh37
NC_000007.12:g.86971138A>G	NCBI36
NG_011513.1:g.214363T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.*357T>C	ENSP00000265724.3:n.*357T>C
ENST00000622132.5:c.*357T>C MANE Select	ENSP00000478255.1:n.*357T>C
ENST00000265724.7:c.*357T>C	ENSP00000265724.3:n.*357T>C
ENST00000488737.6:n.1842T>C
ENST00000543898.5:c.*357T>C	ENSP00000444095.1:n.*357T>C
ENST00000622132.4:c.*357T>C	ENSP00000478255.1:n.*357T>C
NM_000927.4:c.*357T>C	NP_000918.2:n.*357T>C
NM_001348944.1:c.*357T>C	NP_001335873.1:n.*357T>C
NM_001348945.1:c.*357T>C	NP_001335874.1:n.*357T>C
NM_001348946.1:c.*357T>C	NP_001335875.1:n.*357T>C
NM_001348946.2:c.*357T>C MANE Select	NP_001335875.1:n.*357T>C
NM_000927.5:c.*357T>C	NP_000918.2:n.*357T>C
NM_001348944.2:c.*357T>C	NP_001335873.1:n.*357T>C
NM_001348945.2:c.*357T>C	NP_001335874.1:n.*357T>C