Canonical Allele Identifier: CA314388164
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs11536940

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349233G>A , CM000682.2:g.38349233G>A GRCh38
NC_000020.10:g.36977636G>A , CM000682.1:g.36977636G>A GRCh37
NC_000020.9:g.36411050G>A NCBI36
NG_034239.1:g.7823G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-315G>A MANE Select ENSP00000217407.2:n.125-315G>A
ENST00000217407.2:c.125-315G>A ENSP00000217407.2:n.125-315G>A
NM_004139.4:c.125-315G>A NP_004130.2:n.125-315G>A
NM_004139.5:c.125-315G>A MANE Select NP_004130.2:n.125-315G>A