Canonical Allele Identifier: CA314397285

Gene: LBP

Linked Data

• dbSNP Id: rs1041884263
• MyVariant Identifiers: chr20:g.36992226G>A (hg19) ; chr20:g.38363572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38363572G>A , CM000682.2:g.38363572G>A	GRCh38
NC_000020.10:g.36992226G>A , CM000682.1:g.36992226G>A	GRCh37
NC_000020.9:g.36425640G>A	NCBI36
NG_034239.1:g.22162G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217407.3:c.653-403G>A MANE Select	ENSP00000217407.2:n.653-403G>A
ENST00000217407.2:c.653-403G>A	ENSP00000217407.2:n.653-403G>A
NM_004139.4:c.653-403G>A	NP_004130.2:n.653-403G>A
NM_004139.5:c.653-403G>A MANE Select	NP_004130.2:n.653-403G>A