Canonical Allele Identifier: CA2362973144
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363479T= , CM000682.2:g.38363479T= GRCh38
NC_000020.10:g.36992133T= , CM000682.1:g.36992133T= GRCh37
NC_000020.9:g.36425547T= NCBI36
NG_034239.1:g.22069T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-496T= MANE Select ENSP00000217407.2:n.653-496T=
ENST00000217407.2:c.653-496T= ENSP00000217407.2:n.653-496T=
NM_004139.4:c.653-496T= NP_004130.2:n.653-496T=
NM_004139.5:c.653-496T= MANE Select NP_004130.2:n.653-496T=