Canonical Allele Identifier: CA744174852

Gene: LBP

Linked Data

• dbSNP Id: rs1260808078
• gnomAD v3: 20-38363301-G-C
• gnomAD v4: 20-38363301-G-C
• MyVariant Identifiers: chr20:g.36991955G>C (hg19) ; chr20:g.38363301G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38363301G>C , CM000682.2:g.38363301G>C	GRCh38
NC_000020.10:g.36991955G>C , CM000682.1:g.36991955G>C	GRCh37
NC_000020.9:g.36425369G>C	NCBI36
NG_034239.1:g.21891G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217407.3:c.653-674G>C MANE Select	ENSP00000217407.2:n.653-674G>C
ENST00000217407.2:c.653-674G>C	ENSP00000217407.2:n.653-674G>C
NM_004139.4:c.653-674G>C	NP_004130.2:n.653-674G>C
NM_004139.5:c.653-674G>C MANE Select	NP_004130.2:n.653-674G>C