Canonical Allele Identifier: CA314388179
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs952238997
gnomAD v3: 20-38349261-C-T
gnomAD v4: 20-38349261-C-T
MyVariant Identifiers: chr20:g.36977664C>T (hg19) chr20:g.38349261C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349261C>T , CM000682.2:g.38349261C>T GRCh38
NC_000020.10:g.36977664C>T , CM000682.1:g.36977664C>T GRCh37
NC_000020.9:g.36411078C>T NCBI36
NG_034239.1:g.7851C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-287C>T MANE Select ENSP00000217407.2:n.125-287C>T
ENST00000217407.2:c.125-287C>T ENSP00000217407.2:n.125-287C>T
NM_004139.4:c.125-287C>T NP_004130.2:n.125-287C>T
NM_004139.5:c.125-287C>T MANE Select NP_004130.2:n.125-287C>T
Search 100 bp 5'
Search 100 bp 3'