Canonical Allele Identifier: CA1723621299

Gene: ABCB1

Linked Data

• dbSNP Id: rs1814596773
• gnomAD v3: 7-87503890-A-G
• gnomAD v4: 7-87503890-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503890A>G , CM000669.2:g.87503890A>G	GRCh38
NC_000007.13:g.87133206A>G , CM000669.1:g.87133206A>G	GRCh37
NC_000007.12:g.86971142A>G	NCBI36
NG_011513.1:g.214359T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.*353T>C	ENSP00000265724.3:n.*353T>C
ENST00000622132.5:c.*353T>C MANE Select	ENSP00000478255.1:n.*353T>C
ENST00000265724.7:c.*353T>C	ENSP00000265724.3:n.*353T>C
ENST00000488737.6:n.1838T>C
ENST00000543898.5:c.*353T>C	ENSP00000444095.1:n.*353T>C
ENST00000622132.4:c.*353T>C	ENSP00000478255.1:n.*353T>C
NM_000927.4:c.*353T>C	NP_000918.2:n.*353T>C
NM_001348944.1:c.*353T>C	NP_001335873.1:n.*353T>C
NM_001348945.1:c.*353T>C	NP_001335874.1:n.*353T>C
NM_001348946.1:c.*353T>C	NP_001335875.1:n.*353T>C
NM_001348946.2:c.*353T>C MANE Select	NP_001335875.1:n.*353T>C
NM_000927.5:c.*353T>C	NP_000918.2:n.*353T>C
NM_001348944.2:c.*353T>C	NP_001335873.1:n.*353T>C
NM_001348945.2:c.*353T>C	NP_001335874.1:n.*353T>C