Canonical Allele Identifier: CA1769104181
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069976351

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955557C>A , CM000670.2:g.19955557C>A GRCh38
NC_000008.10:g.19813068C>A , CM000670.1:g.19813068C>A GRCh37
NC_000008.9:g.19857348C>A NCBI36
NG_008855.1:g.21487C>A
NG_008855.2:g.58841C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-284C>A MANE Select ENSP00000497642.1:n.776-284C>A
ENST00000311322.8:c.776-284C>A ENSP00000309757.6:n.776-284C>A
NM_000237.2:c.776-284C>A NP_000228.1:n.776-284C>A
NM_000237.3:c.776-284C>A MANE Select NP_000228.1:n.776-284C>A