Canonical Allele Identifier: CA2816323036
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363558G>T , CM000682.2:g.38363558G>T GRCh38
NC_000020.10:g.36992212G>T , CM000682.1:g.36992212G>T GRCh37
NC_000020.9:g.36425626G>T NCBI36
NG_034239.1:g.22148G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-417G>T MANE Select ENSP00000217407.2:n.653-417G>T
ENST00000217407.2:c.653-417G>T ENSP00000217407.2:n.653-417G>T
NM_004139.4:c.653-417G>T NP_004130.2:n.653-417G>T
NM_004139.5:c.653-417G>T MANE Select NP_004130.2:n.653-417G>T