Canonical Allele Identifier: CA1769116670
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070094892
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966962C>G , CM000670.2:g.19966962C>G GRCh38
NC_000008.10:g.19824473C>G , CM000670.1:g.19824473C>G GRCh37
NC_000008.9:g.19868753C>G NCBI36
NG_008855.1:g.32892C>G
NG_008855.2:g.70246C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1652C>G MANE Select ENSP00000497642.1:n.*1652C>G
ENST00000650478.1:c.2020C>G ENSP00000497560.1:n.2020C>G
ENST00000311322.8:c.*1652C>G ENSP00000309757.6:n.*1652C>G
NM_000237.2:c.*1652C>G NP_000228.1:n.*1652C>G
NM_000237.3:c.*1652C>G MANE Select NP_000228.1:n.*1652C>G
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