Canonical Allele Identifier: CA575862188

Gene: ABCB1

Linked Data

• dbSNP Id: rs1404095581
• gnomAD v2: 7-87166053-C-A
• gnomAD v3: 7-87536737-C-A
• gnomAD v4: 7-87536737-C-A
• MyVariant Identifiers: chr7:g.87166053C>A (hg19) ; chr7:g.87536737C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87536737C>A , CM000669.2:g.87536737C>A	GRCh38
NC_000007.13:g.87166053C>A , CM000669.1:g.87166053C>A	GRCh37
NC_000007.12:g.87003989C>A	NCBI36
NG_011513.1:g.181512G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2398-196G>T	ENSP00000265724.3:n.2398-196G>T
ENST00000622132.5:c.2398-196G>T MANE Select	ENSP00000478255.1:n.2398-196G>T
ENST00000265724.7:c.2398-196G>T	ENSP00000265724.3:n.2398-196G>T
ENST00000496821.5:n.26-196G>T
ENST00000543898.5:c.2206-196G>T	ENSP00000444095.1:n.2206-196G>T
ENST00000622132.4:c.2398-196G>T	ENSP00000478255.1:n.2398-196G>T
NM_000927.4:c.2398-196G>T	NP_000918.2:n.2398-196G>T
NM_001348944.1:c.2398-196G>T	NP_001335873.1:n.2398-196G>T
NM_001348945.1:c.2608-196G>T	NP_001335874.1:n.2608-196G>T
NM_001348946.1:c.2398-196G>T	NP_001335875.1:n.2398-196G>T
NM_001348946.2:c.2398-196G>T MANE Select	NP_001335875.1:n.2398-196G>T
NM_000927.5:c.2398-196G>T	NP_000918.2:n.2398-196G>T
NM_001348944.2:c.2398-196G>T	NP_001335873.1:n.2398-196G>T
NM_001348945.2:c.2608-196G>T	NP_001335874.1:n.2608-196G>T