Canonical Allele Identifier: CA314397141

Gene: LBP

Linked Data

• dbSNP Id: rs780075369
• gnomAD v2: 20-36991809-A-G
• gnomAD v3: 20-38363155-A-G
• gnomAD v4: 20-38363155-A-G
• MyVariant Identifiers: chr20:g.36991809A>G (hg19) ; chr20:g.38363155A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38363155A>G , CM000682.2:g.38363155A>G	GRCh38
NC_000020.10:g.36991809A>G , CM000682.1:g.36991809A>G	GRCh37
NC_000020.9:g.36425223A>G	NCBI36
NG_034239.1:g.21745A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217407.3:c.653-820A>G MANE Select	ENSP00000217407.2:n.653-820A>G
ENST00000217407.2:c.653-820A>G	ENSP00000217407.2:n.653-820A>G
NM_004139.4:c.653-820A>G	NP_004130.2:n.653-820A>G
NM_004139.5:c.653-820A>G MANE Select	NP_004130.2:n.653-820A>G