Canonical Allele Identifier: CA2362966305
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349244C= , CM000682.2:g.38349244C= GRCh38
NC_000020.10:g.36977647C= , CM000682.1:g.36977647C= GRCh37
NC_000020.9:g.36411061C= NCBI36
NG_034239.1:g.7834C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-304C= MANE Select ENSP00000217407.2:n.125-304C=
ENST00000217407.2:c.125-304C= ENSP00000217407.2:n.125-304C=
NM_004139.4:c.125-304C= NP_004130.2:n.125-304C=
NM_004139.5:c.125-304C= MANE Select NP_004130.2:n.125-304C=