Canonical Allele Identifier: CA2362966318
Gene: LBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349264C= , CM000682.2:g.38349264C= GRCh38
NC_000020.10:g.36977667C= , CM000682.1:g.36977667C= GRCh37
NC_000020.9:g.36411081C= NCBI36
NG_034239.1:g.7854C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-284C= MANE Select ENSP00000217407.2:n.125-284C=
ENST00000217407.2:c.125-284C= ENSP00000217407.2:n.125-284C=
NM_004139.4:c.125-284C= NP_004130.2:n.125-284C=
NM_004139.5:c.125-284C= MANE Select NP_004130.2:n.125-284C=
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