Canonical Allele Identifier: CA314397150
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs563003634

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363172G>C , CM000682.2:g.38363172G>C GRCh38
NC_000020.10:g.36991826G>C , CM000682.1:g.36991826G>C GRCh37
NC_000020.9:g.36425240G>C NCBI36
NG_034239.1:g.21762G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-803G>C MANE Select ENSP00000217407.2:n.653-803G>C
ENST00000217407.2:c.653-803G>C ENSP00000217407.2:n.653-803G>C
NM_004139.4:c.653-803G>C NP_004130.2:n.653-803G>C
NM_004139.5:c.653-803G>C MANE Select NP_004130.2:n.653-803G>C