Canonical Allele Identifier: CA314397157
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs949759161
gnomAD v2: 20-36991923-T-G
gnomAD v3: 20-38363269-T-G
gnomAD v4: 20-38363269-T-G
MyVariant Identifiers: chr20:g.36991923T>G (hg19) chr20:g.38363269T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363269T>G , CM000682.2:g.38363269T>G GRCh38
NC_000020.10:g.36991923T>G , CM000682.1:g.36991923T>G GRCh37
NC_000020.9:g.36425337T>G NCBI36
NG_034239.1:g.21859T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-706T>G MANE Select ENSP00000217407.2:n.653-706T>G
ENST00000217407.2:c.653-706T>G ENSP00000217407.2:n.653-706T>G
NM_004139.4:c.653-706T>G NP_004130.2:n.653-706T>G
NM_004139.5:c.653-706T>G MANE Select NP_004130.2:n.653-706T>G
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