Canonical Allele Identifier: CA162107573

Gene: ABCB1

Linked Data

• dbSNP Id: rs922356325
• MyVariant Identifiers: chr7:g.87152107del (hg19) ; chr7:g.87522791del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87522797del , CM000669.2:g.87522797del	GRCh38
NC_000007.13:g.87152113del , CM000669.1:g.87152113del	GRCh37
NC_000007.12:g.86990049del	NCBI36
NG_011513.1:g.195458del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2686-1915del	ENSP00000265724.3:n.2686-1915del
ENST00000622132.5:c.2686-1915del MANE Select	ENSP00000478255.1:n.2686-1915del
ENST00000265724.7:c.2686-1915del	ENSP00000265724.3:n.2686-1915del
ENST00000488737.6:n.328-1915del
ENST00000496821.5:n.314-1915del
ENST00000543898.5:c.2494-1915del	ENSP00000444095.1:n.2494-1915del
ENST00000622132.4:c.2686-1915del	ENSP00000478255.1:n.2686-1915del
NM_000927.4:c.2686-1915del	NP_000918.2:n.2686-1915del
NM_001348944.1:c.2686-1915del	NP_001335873.1:n.2686-1915del
NM_001348945.1:c.2896-1915del	NP_001335874.1:n.2896-1915del
NM_001348946.1:c.2686-1915del	NP_001335875.1:n.2686-1915del
NM_001348946.2:c.2686-1915del MANE Select	NP_001335875.1:n.2686-1915del
NM_000927.5:c.2686-1915del	NP_000918.2:n.2686-1915del
NM_001348944.2:c.2686-1915del	NP_001335873.1:n.2686-1915del
NM_001348945.2:c.2896-1915del	NP_001335874.1:n.2896-1915del