Canonical Allele Identifier: CA370468825
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811866T>A (hg19) chr8:g.19954355T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954355T>A , CM000670.2:g.19954355T>A GRCh38
NC_000008.10:g.19811866T>A , CM000670.1:g.19811866T>A GRCh37
NC_000008.9:g.19856146T>A NCBI36
NG_008855.1:g.20285T>A
NG_008855.2:g.57639T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+2T>A MANE Select ENSP00000497642.1:n.775+2T>A
ENST00000311322.8:c.775+2T>A ENSP00000309757.6:n.775+2T>A
NM_000237.2:c.775+2T>A NP_000228.1:n.775+2T>A
NM_000237.3:c.775+2T>A MANE Select NP_000228.1:n.775+2T>A
Search 100 bp 5'
Search 100 bp 3'