Canonical Allele Identifier: CA4655528
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs755438453
gnomAD v2: 8-19813310-A-G
gnomAD v4: 8-19955799-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955799A>G , CM000670.2:g.19955799A>G GRCh38
NC_000008.10:g.19813310A>G , CM000670.1:g.19813310A>G GRCh37
NC_000008.9:g.19857590A>G NCBI36
NG_008855.1:g.21729A>G
NG_008855.2:g.59083A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-42A>G MANE Select ENSP00000497642.1:n.776-42A>G
ENST00000311322.8:c.776-42A>G ENSP00000309757.6:n.776-42A>G
NM_000237.2:c.776-42A>G NP_000228.1:n.776-42A>G
NM_000237.3:c.776-42A>G MANE Select NP_000228.1:n.776-42A>G