Canonical Allele Identifier: CA459879715
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813546A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956035A>C , CM000670.2:g.19956035A>C GRCh38
NC_000008.10:g.19813546A>C , CM000670.1:g.19813546A>C GRCh37
NC_000008.9:g.19857826A>C NCBI36
NG_008855.1:g.21965A>C
NG_008855.2:g.59319A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.970A>C MANE Select ENSP00000497642.1:p.Arg324=
ENST00000650478.1:c.31A>C ENSP00000497560.1:p.Arg11=
ENST00000311322.8:c.970A>C ENSP00000309757.6:p.Arg324=
NM_000237.2:c.970A>C NP_000228.1:p.Arg324=
NM_000237.3:c.970A>C MANE Select NP_000228.1:p.Arg324=
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Search 100 bp 3'