Canonical Allele Identifier: CA456449955

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87179302C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87549986C>G , CM000669.2:g.87549986C>G	GRCh38
NC_000007.13:g.87179302C>G , CM000669.1:g.87179302C>G	GRCh37
NC_000007.12:g.87017238C>G	NCBI36
NG_011513.1:g.168263G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1419G>C	ENSP00000265724.3:p.Val473=
ENST00000622132.5:c.1419G>C MANE Select	ENSP00000478255.1:p.Val473=
ENST00000265724.7:c.1419G>C	ENSP00000265724.3:p.Val473=
ENST00000482527.1:n.173G>C
ENST00000543898.5:c.1227G>C	ENSP00000444095.1:p.Val409=
ENST00000622132.4:c.1419G>C	ENSP00000478255.1:p.Val473=
NM_000927.4:c.1419G>C	NP_000918.2:p.Val473=
NM_001348944.1:c.1419G>C	NP_001335873.1:p.Val473=
NM_001348945.1:c.1629G>C	NP_001335874.1:p.Val543=
NM_001348946.1:c.1419G>C	NP_001335875.1:p.Val473=
NM_001348946.2:c.1419G>C MANE Select	NP_001335875.1:p.Val473=
NM_000927.5:c.1419G>C	NP_000918.2:p.Val473=
NM_001348944.2:c.1419G>C	NP_001335873.1:p.Val473=
NM_001348945.2:c.1629G>C	NP_001335874.1:p.Val543=