Canonical Allele Identifier: CA635443662

Gene: LBP

Linked Data

• dbSNP Id: rs1169419032
• gnomAD v2: 20-36992035-C-T
• gnomAD v3: 20-38363381-C-T
• gnomAD v4: 20-38363381-C-T
• MyVariant Identifiers: chr20:g.36992035C>T (hg19) ; chr20:g.38363381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38363381C>T , CM000682.2:g.38363381C>T	GRCh38
NC_000020.10:g.36992035C>T , CM000682.1:g.36992035C>T	GRCh37
NC_000020.9:g.36425449C>T	NCBI36
NG_034239.1:g.21971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217407.3:c.653-594C>T MANE Select	ENSP00000217407.2:n.653-594C>T
ENST00000217407.2:c.653-594C>T	ENSP00000217407.2:n.653-594C>T
NM_004139.4:c.653-594C>T	NP_004130.2:n.653-594C>T
NM_004139.5:c.653-594C>T MANE Select	NP_004130.2:n.653-594C>T