Canonical Allele Identifier: CA314397282
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs113464344
gnomAD v2: 20-36992220-G-A
gnomAD v3: 20-38363566-G-A
gnomAD v4: 20-38363566-G-A
MyVariant Identifiers: chr20:g.36992220G>A (hg19) chr20:g.38363566G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363566G>A , CM000682.2:g.38363566G>A GRCh38
NC_000020.10:g.36992220G>A , CM000682.1:g.36992220G>A GRCh37
NC_000020.9:g.36425634G>A NCBI36
NG_034239.1:g.22156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-409G>A MANE Select ENSP00000217407.2:n.653-409G>A
ENST00000217407.2:c.653-409G>A ENSP00000217407.2:n.653-409G>A
NM_004139.4:c.653-409G>A NP_004130.2:n.653-409G>A
NM_004139.5:c.653-409G>A MANE Select NP_004130.2:n.653-409G>A
Search 100 bp 5'
Search 100 bp 3'