Canonical Allele Identifier: CA2362973162
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs2076869101
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363510C>A , CM000682.2:g.38363510C>A GRCh38
NC_000020.10:g.36992164C>A , CM000682.1:g.36992164C>A GRCh37
NC_000020.9:g.36425578C>A NCBI36
NG_034239.1:g.22100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-465C>A MANE Select ENSP00000217407.2:n.653-465C>A
ENST00000217407.2:c.653-465C>A ENSP00000217407.2:n.653-465C>A
NM_004139.4:c.653-465C>A NP_004130.2:n.653-465C>A
NM_004139.5:c.653-465C>A MANE Select NP_004130.2:n.653-465C>A
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