Canonical Allele Identifier: CA2362966321
Gene: LBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349273C= , CM000682.2:g.38349273C= GRCh38
NC_000020.10:g.36977676C= , CM000682.1:g.36977676C= GRCh37
NC_000020.9:g.36411090C= NCBI36
NG_034239.1:g.7863C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-275C= MANE Select ENSP00000217407.2:n.125-275C=
ENST00000217407.2:c.125-275C= ENSP00000217407.2:n.125-275C=
NM_004139.4:c.125-275C= NP_004130.2:n.125-275C=
NM_004139.5:c.125-275C= MANE Select NP_004130.2:n.125-275C=
Search 100 bp 5'
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