Canonical Allele Identifier: CA162112827

Gene: ABCB1

Linked Data

• dbSNP Id: rs926775991
• gnomAD v2: 7-87164956-G-C
• gnomAD v3: 7-87535640-G-C
• gnomAD v4: 7-87535640-G-C
• MyVariant Identifiers: chr7:g.87164956G>C (hg19) ; chr7:g.87535640G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87535640G>C , CM000669.2:g.87535640G>C	GRCh38
NC_000007.13:g.87164956G>C , CM000669.1:g.87164956G>C	GRCh37
NC_000007.12:g.87002892G>C	NCBI36
NG_011513.1:g.182609C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2481+818C>G	ENSP00000265724.3:n.2481+818C>G
ENST00000622132.5:c.2481+818C>G MANE Select	ENSP00000478255.1:n.2481+818C>G
ENST00000265724.7:c.2481+818C>G	ENSP00000265724.3:n.2481+818C>G
ENST00000496821.5:n.109+818C>G
ENST00000543898.5:c.2289+818C>G	ENSP00000444095.1:n.2289+818C>G
ENST00000622132.4:c.2481+818C>G	ENSP00000478255.1:n.2481+818C>G
NM_000927.4:c.2481+818C>G	NP_000918.2:n.2481+818C>G
NM_001348944.1:c.2481+818C>G	NP_001335873.1:n.2481+818C>G
NM_001348945.1:c.2691+818C>G	NP_001335874.1:n.2691+818C>G
NM_001348946.1:c.2481+818C>G	NP_001335875.1:n.2481+818C>G
NM_001348946.2:c.2481+818C>G MANE Select	NP_001335875.1:n.2481+818C>G
NM_000927.5:c.2481+818C>G	NP_000918.2:n.2481+818C>G
NM_001348944.2:c.2481+818C>G	NP_001335873.1:n.2481+818C>G
NM_001348945.2:c.2691+818C>G	NP_001335874.1:n.2691+818C>G