Canonical Allele Identifier: CA635443654
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs1181176001
gnomAD v2: 20-36991998-C-G
gnomAD v3: 20-38363344-C-G
gnomAD v4: 20-38363344-C-G
MyVariant Identifiers: chr20:g.36991998C>G (hg19) chr20:g.38363344C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363344C>G , CM000682.2:g.38363344C>G GRCh38
NC_000020.10:g.36991998C>G , CM000682.1:g.36991998C>G GRCh37
NC_000020.9:g.36425412C>G NCBI36
NG_034239.1:g.21934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-631C>G MANE Select ENSP00000217407.2:n.653-631C>G
ENST00000217407.2:c.653-631C>G ENSP00000217407.2:n.653-631C>G
NM_004139.4:c.653-631C>G NP_004130.2:n.653-631C>G
NM_004139.5:c.653-631C>G MANE Select NP_004130.2:n.653-631C>G
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