Canonical Allele Identifier: CA459879482
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811755A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954244A>G , CM000670.2:g.19954244A>G GRCh38
NC_000008.10:g.19811755A>G , CM000670.1:g.19811755A>G GRCh37
NC_000008.9:g.19856035A>G NCBI36
NG_008855.1:g.20174A>G
NG_008855.2:g.57528A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.666A>G MANE Select ENSP00000497642.1:p.Gly222=
ENST00000311322.8:c.666A>G ENSP00000309757.6:p.Gly222=
NM_000237.2:c.666A>G NP_000228.1:p.Gly222=
NM_000237.3:c.666A>G MANE Select NP_000228.1:p.Gly222=
Search 100 bp 5'
Search 100 bp 3'