Canonical Allele Identifier: CA368046784

Gene: ABCB1

Linked Data

• MyVariant Identifiers: chr7:g.87145875T>G (hg19) ; chr7:g.87516559T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516559T>G , CM000669.2:g.87516559T>G	GRCh38
NC_000007.13:g.87145875T>G , CM000669.1:g.87145875T>G	GRCh37
NC_000007.12:g.86983811T>G	NCBI36
NG_011513.1:g.201690A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3034A>C	ENSP00000265724.3:p.Ile1012Leu
ENST00000622132.5:c.3034A>C MANE Select	ENSP00000478255.1:p.Ile1012Leu
ENST00000265724.7:c.3034A>C	ENSP00000265724.3:p.Ile1012Leu
ENST00000475929.5:n.190A>C
ENST00000483831.1:n.592A>C
ENST00000488737.6:n.676A>C
ENST00000496821.5:n.662A>C
ENST00000543898.5:c.2842A>C	ENSP00000444095.1:p.Ile948Leu
ENST00000622132.4:c.3034A>C	ENSP00000478255.1:p.Ile1012Leu
NM_000927.4:c.3034A>C	NP_000918.2:p.Ile1012Leu
NM_001348944.1:c.3034A>C	NP_001335873.1:p.Ile1012Leu
NM_001348945.1:c.3244A>C	NP_001335874.1:p.Ile1082Leu
NM_001348946.1:c.3034A>C	NP_001335875.1:p.Ile1012Leu
NM_001348946.2:c.3034A>C MANE Select	NP_001335875.1:p.Ile1012Leu
NM_000927.5:c.3034A>C	NP_000918.2:p.Ile1012Leu
NM_001348944.2:c.3034A>C	NP_001335873.1:p.Ile1012Leu
NM_001348945.2:c.3244A>C	NP_001335874.1:p.Ile1082Leu