Canonical Allele Identifier: CA173618079
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs757883454
gnomAD v2: 8-19819384-C-G
gnomAD v3: 8-19961873-C-G
gnomAD v4: 8-19961873-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961873C>G , CM000670.2:g.19961873C>G GRCh38
NC_000008.10:g.19819384C>G , CM000670.1:g.19819384C>G GRCh37
NC_000008.9:g.19863664C>G NCBI36
NG_008855.1:g.27803C>G
NG_008855.2:g.65157C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1323-242C>G MANE Select ENSP00000497642.1:n.1323-242C>G
ENST00000650478.1:c.263-242C>G ENSP00000497560.1:n.263-242C>G
ENST00000311322.8:c.1323-242C>G ENSP00000309757.6:n.1323-242C>G
NM_000237.2:c.1323-242C>G NP_000228.1:n.1323-242C>G
NM_000237.3:c.1323-242C>G MANE Select NP_000228.1:n.1323-242C>G