Canonical Allele Identifier: CA2362973036
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363282A= , CM000682.2:g.38363282A= GRCh38
NC_000020.10:g.36991936A= , CM000682.1:g.36991936A= GRCh37
NC_000020.9:g.36425350A= NCBI36
NG_034239.1:g.21872A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-693A= MANE Select ENSP00000217407.2:n.653-693A=
ENST00000217407.2:c.653-693A= ENSP00000217407.2:n.653-693A=
NM_004139.4:c.653-693A= NP_004130.2:n.653-693A=
NM_004139.5:c.653-693A= MANE Select NP_004130.2:n.653-693A=