Canonical Allele Identifier: CA635438076
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs368199844
gnomAD v2: 20-37001684-G-C
gnomAD v4: 20-38373040-G-C
MyVariant Identifiers: chr20:g.37001684G>C (hg19) chr20:g.38373040G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38373040G>C , CM000682.2:g.38373040G>C GRCh38
NC_000020.10:g.37001684G>C , CM000682.1:g.37001684G>C GRCh37
NC_000020.9:g.36435098G>C NCBI36
NG_034239.1:g.31630G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.1261-32G>C MANE Select ENSP00000217407.2:n.1261-32G>C
ENST00000217407.2:c.1261-32G>C ENSP00000217407.2:n.1261-32G>C
NM_004139.4:c.1261-32G>C NP_004130.2:n.1261-32G>C
NM_004139.5:c.1261-32G>C MANE Select NP_004130.2:n.1261-32G>C
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