Canonical Allele Identifier: CA459879438
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813398C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955887C>A , CM000670.2:g.19955887C>A GRCh38
NC_000008.10:g.19813398C>A , CM000670.1:g.19813398C>A GRCh37
NC_000008.9:g.19857678C>A NCBI36
NG_008855.1:g.21817C>A
NG_008855.2:g.59171C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.822C>A MANE Select ENSP00000497642.1:p.Leu274=
ENST00000311322.8:c.822C>A ENSP00000309757.6:p.Leu274=
NM_000237.2:c.822C>A NP_000228.1:p.Leu274=
NM_000237.3:c.822C>A MANE Select NP_000228.1:p.Leu274=
Search 100 bp 5'
Search 100 bp 3'