Canonical Allele Identifier: CA1017419570
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs2076868857
gnomAD v3: 20-38363458-G-C
gnomAD v4: 20-38363458-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363458G>C , CM000682.2:g.38363458G>C GRCh38
NC_000020.10:g.36992112G>C , CM000682.1:g.36992112G>C GRCh37
NC_000020.9:g.36425526G>C NCBI36
NG_034239.1:g.22048G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-517G>C MANE Select ENSP00000217407.2:n.653-517G>C
ENST00000217407.2:c.653-517G>C ENSP00000217407.2:n.653-517G>C
NM_004139.4:c.653-517G>C NP_004130.2:n.653-517G>C
NM_004139.5:c.653-517G>C MANE Select NP_004130.2:n.653-517G>C
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