Canonical Allele Identifier: CA2362977720
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38373023C= , CM000682.2:g.38373023C= GRCh38
NC_000020.10:g.37001667C= , CM000682.1:g.37001667C= GRCh37
NC_000020.9:g.36435081C= NCBI36
NG_034239.1:g.31613C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.1261-49C= MANE Select ENSP00000217407.2:n.1261-49C=
ENST00000217407.2:c.1261-49C= ENSP00000217407.2:n.1261-49C=
NM_004139.4:c.1261-49C= NP_004130.2:n.1261-49C=
NM_004139.5:c.1261-49C= MANE Select NP_004130.2:n.1261-49C=