Canonical Allele Identifier: CA2362973188
Gene: LBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363572G= , CM000682.2:g.38363572G= GRCh38
NC_000020.10:g.36992226G= , CM000682.1:g.36992226G= GRCh37
NC_000020.9:g.36425640G= NCBI36
NG_034239.1:g.22162G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-403G= MANE Select ENSP00000217407.2:n.653-403G=
ENST00000217407.2:c.653-403G= ENSP00000217407.2:n.653-403G=
NM_004139.4:c.653-403G= NP_004130.2:n.653-403G=
NM_004139.5:c.653-403G= MANE Select NP_004130.2:n.653-403G=
Search 100 bp 5'
Search 100 bp 3'