Canonical Allele Identifier: CA2362966304
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349239G= , CM000682.2:g.38349239G= GRCh38
NC_000020.10:g.36977642G= , CM000682.1:g.36977642G= GRCh37
NC_000020.9:g.36411056G= NCBI36
NG_034239.1:g.7829G=

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-309G= MANE Select ENSP00000217407.2:n.125-309G=
ENST00000217407.2:c.125-309G= ENSP00000217407.2:n.125-309G=
NM_004139.4:c.125-309G= NP_004130.2:n.125-309G=
NM_004139.5:c.125-309G= MANE Select NP_004130.2:n.125-309G=