Canonical Allele Identifier: CA2362973183
Gene: LBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363565C= , CM000682.2:g.38363565C= GRCh38
NC_000020.10:g.36992219C= , CM000682.1:g.36992219C= GRCh37
NC_000020.9:g.36425633C= NCBI36
NG_034239.1:g.22155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-410C= MANE Select ENSP00000217407.2:n.653-410C=
ENST00000217407.2:c.653-410C= ENSP00000217407.2:n.653-410C=
NM_004139.4:c.653-410C= NP_004130.2:n.653-410C=
NM_004139.5:c.653-410C= MANE Select NP_004130.2:n.653-410C=
Search 100 bp 5'
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