Canonical Allele Identifier: CA370469051
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813409C>A (hg19) chr8:g.19955898C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955898C>A , CM000670.2:g.19955898C>A GRCh38
NC_000008.10:g.19813409C>A , CM000670.1:g.19813409C>A GRCh37
NC_000008.9:g.19857689C>A NCBI36
NG_008855.1:g.21828C>A
NG_008855.2:g.59182C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.833C>A MANE Select ENSP00000497642.1:p.Ser278Tyr
ENST00000311322.8:c.833C>A ENSP00000309757.6:p.Ser278Tyr
NM_000237.2:c.833C>A NP_000228.1:p.Ser278Tyr
NM_000237.3:c.833C>A MANE Select NP_000228.1:p.Ser278Tyr
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