Canonical Allele Identifier: CA1769112708
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590149204
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962956T>A , CM000670.2:g.19962956T>A GRCh38
NC_000008.10:g.19820467T>A , CM000670.1:g.19820467T>A GRCh37
NC_000008.9:g.19864747T>A NCBI36
NG_008855.1:g.28886T>A
NG_008855.2:g.66240T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1427+737T>A MANE Select ENSP00000497642.1:n.1427+737T>A
ENST00000650478.1:c.367+737T>A ENSP00000497560.1:n.367+737T>A
ENST00000311322.8:c.1427+737T>A ENSP00000309757.6:n.1427+737T>A
NM_000237.2:c.1427+737T>A NP_000228.1:n.1427+737T>A
NM_000237.3:c.1427+737T>A MANE Select NP_000228.1:n.1427+737T>A
Search 100 bp 5'
Search 100 bp 3'