Canonical Allele Identifier: CA744174827
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs1213618278
gnomAD v3: 20-38363163-A-G
gnomAD v4: 20-38363163-A-G
MyVariant Identifiers: chr20:g.36991817A>G (hg19) chr20:g.38363163A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363163A>G , CM000682.2:g.38363163A>G GRCh38
NC_000020.10:g.36991817A>G , CM000682.1:g.36991817A>G GRCh37
NC_000020.9:g.36425231A>G NCBI36
NG_034239.1:g.21753A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-812A>G MANE Select ENSP00000217407.2:n.653-812A>G
ENST00000217407.2:c.653-812A>G ENSP00000217407.2:n.653-812A>G
NM_004139.4:c.653-812A>G NP_004130.2:n.653-812A>G
NM_004139.5:c.653-812A>G MANE Select NP_004130.2:n.653-812A>G
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