Canonical Allele Identifier: CA2362973029
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363273A= , CM000682.2:g.38363273A= GRCh38
NC_000020.10:g.36991927A= , CM000682.1:g.36991927A= GRCh37
NC_000020.9:g.36425341A= NCBI36
NG_034239.1:g.21863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-702A= MANE Select ENSP00000217407.2:n.653-702A=
ENST00000217407.2:c.653-702A= ENSP00000217407.2:n.653-702A=
NM_004139.4:c.653-702A= NP_004130.2:n.653-702A=
NM_004139.5:c.653-702A= MANE Select NP_004130.2:n.653-702A=