Canonical Allele Identifier: CA370468517
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1419888659
gnomAD v2: 8-19811759-C-G
gnomAD v3: 8-19954248-C-G
gnomAD v4: 8-19954248-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954248C>G , CM000670.2:g.19954248C>G GRCh38
NC_000008.10:g.19811759C>G , CM000670.1:g.19811759C>G GRCh37
NC_000008.9:g.19856039C>G NCBI36
NG_008855.1:g.20178C>G
NG_008855.2:g.57532C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.670C>G MANE Select ENSP00000497642.1:p.Gln224Glu
ENST00000311322.8:c.670C>G ENSP00000309757.6:p.Gln224Glu
NM_000237.2:c.670C>G NP_000228.1:p.Gln224Glu
NM_000237.3:c.670C>G MANE Select NP_000228.1:p.Gln224Glu