Canonical Allele Identifier: CA368090401

Gene: ABCB1

Linked Data

• COSMIC: COSM3641931
• MyVariant Identifiers: chr7:g.87195442G>A (hg19) ; chr7:g.87566126G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87566126G>A , CM000669.2:g.87566126G>A	GRCh38
NC_000007.13:g.87195442G>A , CM000669.1:g.87195442G>A	GRCh37
NC_000007.12:g.87033378G>A	NCBI36
NG_011513.1:g.152123C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.646C>T	ENSP00000265724.3:p.Leu216Phe
ENST00000622132.5:c.646C>T MANE Select	ENSP00000478255.1:p.Leu216Phe
ENST00000265724.7:c.646C>T	ENSP00000265724.3:p.Leu216Phe
ENST00000543898.5:c.454C>T	ENSP00000444095.1:p.Leu152Phe
ENST00000622132.4:c.646C>T	ENSP00000478255.1:p.Leu216Phe
NM_000927.4:c.646C>T	NP_000918.2:p.Leu216Phe
NM_001348944.1:c.646C>T	NP_001335873.1:p.Leu216Phe
NM_001348945.1:c.856C>T	NP_001335874.1:p.Leu286Phe
NM_001348946.1:c.646C>T	NP_001335875.1:p.Leu216Phe
NM_001348946.2:c.646C>T MANE Select	NP_001335875.1:p.Leu216Phe
NM_000927.5:c.646C>T	NP_000918.2:p.Leu216Phe
NM_001348944.2:c.646C>T	NP_001335873.1:p.Leu216Phe
NM_001348945.2:c.856C>T	NP_001335874.1:p.Leu286Phe