Canonical Allele Identifier: CA368047295

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87516630-A-G
• MyVariant Identifiers: chr7:g.87145946A>G (hg19) ; chr7:g.87516630A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516630A>G , CM000669.2:g.87516630A>G	GRCh38
NC_000007.13:g.87145946A>G , CM000669.1:g.87145946A>G	GRCh37
NC_000007.12:g.86983882A>G	NCBI36
NG_011513.1:g.201619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2963T>C	ENSP00000265724.3:p.Val988Ala
ENST00000622132.5:c.2963T>C MANE Select	ENSP00000478255.1:p.Val988Ala
ENST00000265724.7:c.2963T>C	ENSP00000265724.3:p.Val988Ala
ENST00000475929.5:n.119T>C
ENST00000483831.1:n.521T>C
ENST00000488737.6:n.605T>C
ENST00000496821.5:n.591T>C
ENST00000543898.5:c.2771T>C	ENSP00000444095.1:p.Val924Ala
ENST00000622132.4:c.2963T>C	ENSP00000478255.1:p.Val988Ala
NM_000927.4:c.2963T>C	NP_000918.2:p.Val988Ala
NM_001348944.1:c.2963T>C	NP_001335873.1:p.Val988Ala
NM_001348945.1:c.3173T>C	NP_001335874.1:p.Val1058Ala
NM_001348946.1:c.2963T>C	NP_001335875.1:p.Val988Ala
NM_001348946.2:c.2963T>C MANE Select	NP_001335875.1:p.Val988Ala
NM_000927.5:c.2963T>C	NP_000918.2:p.Val988Ala
NM_001348944.2:c.2963T>C	NP_001335873.1:p.Val988Ala
NM_001348945.2:c.3173T>C	NP_001335874.1:p.Val1058Ala