Canonical Allele Identifier: CA2362973013

Gene: LBP

Linked Data

• dbSNP Id: rs2076867765

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38363210_38363212del , CM000682.2:g.38363210_38363212del	GRCh38
NC_000020.10:g.36991864_36991866del , CM000682.1:g.36991864_36991866del	GRCh37
NC_000020.9:g.36425278_36425280del	NCBI36
NG_034239.1:g.21800_21802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217407.3:c.653-765_653-763del MANE Select	ENSP00000217407.2:n.653-765_653-763del
ENST00000217407.2:c.653-765_653-763del	ENSP00000217407.2:n.653-765_653-763del
NM_004139.4:c.653-765_653-763del	NP_004130.2:n.653-765_653-763del
NM_004139.5:c.653-765_653-763del MANE Select	NP_004130.2:n.653-765_653-763del