Canonical Allele Identifier: CA459879716
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813548A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956037A>G , CM000670.2:g.19956037A>G GRCh38
NC_000008.10:g.19813548A>G , CM000670.1:g.19813548A>G GRCh37
NC_000008.9:g.19857828A>G NCBI36
NG_008855.1:g.21967A>G
NG_008855.2:g.59321A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.972A>G MANE Select ENSP00000497642.1:p.Arg324=
ENST00000650478.1:c.33A>G ENSP00000497560.1:p.Arg11=
ENST00000311322.8:c.972A>G ENSP00000309757.6:p.Arg324=
NM_000237.2:c.972A>G NP_000228.1:p.Arg324=
NM_000237.3:c.972A>G MANE Select NP_000228.1:p.Arg324=
Search 100 bp 5'
Search 100 bp 3'