Canonical Allele Identifier: CA576267678

Gene: ABCB1

Linked Data

• dbSNP Id: rs1323240354
• gnomAD v2: 7-87146133-G-T
• gnomAD v3: 7-87516817-G-T
• gnomAD v4: 7-87516817-G-T
• MyVariant Identifiers: chr7:g.87146133G>T (hg19) ; chr7:g.87516817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516817G>T , CM000669.2:g.87516817G>T	GRCh38
NC_000007.13:g.87146133G>T , CM000669.1:g.87146133G>T	GRCh37
NC_000007.12:g.86984069G>T	NCBI36
NG_011513.1:g.201432C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2928-152C>A	ENSP00000265724.3:n.2928-152C>A
ENST00000622132.5:c.2928-152C>A MANE Select	ENSP00000478255.1:n.2928-152C>A
ENST00000265724.7:c.2928-152C>A	ENSP00000265724.3:n.2928-152C>A
ENST00000475929.5:n.84-152C>A
ENST00000483831.1:n.486-152C>A
ENST00000488737.6:n.570-152C>A
ENST00000496821.5:n.556-152C>A
ENST00000543898.5:c.2736-152C>A	ENSP00000444095.1:n.2736-152C>A
ENST00000622132.4:c.2928-152C>A	ENSP00000478255.1:n.2928-152C>A
NM_000927.4:c.2928-152C>A	NP_000918.2:n.2928-152C>A
NM_001348944.1:c.2928-152C>A	NP_001335873.1:n.2928-152C>A
NM_001348945.1:c.3138-152C>A	NP_001335874.1:n.3138-152C>A
NM_001348946.1:c.2928-152C>A	NP_001335875.1:n.2928-152C>A
NM_001348946.2:c.2928-152C>A MANE Select	NP_001335875.1:n.2928-152C>A
NM_000927.5:c.2928-152C>A	NP_000918.2:n.2928-152C>A
NM_001348944.2:c.2928-152C>A	NP_001335873.1:n.2928-152C>A
NM_001348945.2:c.3138-152C>A	NP_001335874.1:n.3138-152C>A