Canonical Allele Identifier: CA2362973040
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs2076868058
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363288T>G , CM000682.2:g.38363288T>G GRCh38
NC_000020.10:g.36991942T>G , CM000682.1:g.36991942T>G GRCh37
NC_000020.9:g.36425356T>G NCBI36
NG_034239.1:g.21878T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-687T>G MANE Select ENSP00000217407.2:n.653-687T>G
ENST00000217407.2:c.653-687T>G ENSP00000217407.2:n.653-687T>G
NM_004139.4:c.653-687T>G NP_004130.2:n.653-687T>G
NM_004139.5:c.653-687T>G MANE Select NP_004130.2:n.653-687T>G
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