Canonical Allele Identifier: CA459879424
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813389C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955878C>G , CM000670.2:g.19955878C>G GRCh38
NC_000008.10:g.19813389C>G , CM000670.1:g.19813389C>G GRCh37
NC_000008.9:g.19857669C>G NCBI36
NG_008855.1:g.21808C>G
NG_008855.2:g.59162C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.813C>G MANE Select ENSP00000497642.1:p.Ser271=
ENST00000311322.8:c.813C>G ENSP00000309757.6:p.Ser271=
NM_000237.2:c.813C>G NP_000228.1:p.Ser271=
NM_000237.3:c.813C>G MANE Select NP_000228.1:p.Ser271=
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