Canonical Allele Identifier: CA2362973079
Gene: LBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363349T= , CM000682.2:g.38363349T= GRCh38
NC_000020.10:g.36992003T= , CM000682.1:g.36992003T= GRCh37
NC_000020.9:g.36425417T= NCBI36
NG_034239.1:g.21939T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-626T= MANE Select ENSP00000217407.2:n.653-626T=
ENST00000217407.2:c.653-626T= ENSP00000217407.2:n.653-626T=
NM_004139.4:c.653-626T= NP_004130.2:n.653-626T=
NM_004139.5:c.653-626T= MANE Select NP_004130.2:n.653-626T=
Search 100 bp 5'
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