Canonical Allele Identifier: CA2362973182
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363558G= , CM000682.2:g.38363558G= GRCh38
NC_000020.10:g.36992212G= , CM000682.1:g.36992212G= GRCh37
NC_000020.9:g.36425626G= NCBI36
NG_034239.1:g.22148G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-417G= MANE Select ENSP00000217407.2:n.653-417G=
ENST00000217407.2:c.653-417G= ENSP00000217407.2:n.653-417G=
NM_004139.4:c.653-417G= NP_004130.2:n.653-417G=
NM_004139.5:c.653-417G= MANE Select NP_004130.2:n.653-417G=