Canonical Allele Identifier: CA2362966315
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349259T= , CM000682.2:g.38349259T= GRCh38
NC_000020.10:g.36977662T= , CM000682.1:g.36977662T= GRCh37
NC_000020.9:g.36411076T= NCBI36
NG_034239.1:g.7849T=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-289T= MANE Select ENSP00000217407.2:n.125-289T=
ENST00000217407.2:c.125-289T= ENSP00000217407.2:n.125-289T=
NM_004139.4:c.125-289T= NP_004130.2:n.125-289T=
NM_004139.5:c.125-289T= MANE Select NP_004130.2:n.125-289T=