Canonical Allele Identifier: CA4655381
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs537745634
ExAC: 8:19809355 A / G
gnomAD v2: 8-19809355-A-G
gnomAD v3: 8-19951844-A-G
gnomAD v4: 8-19951844-A-G
MyVariant Identifiers: chr8:g.19809355A>G (hg19) chr8:g.19951844A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951844A>G , CM000670.2:g.19951844A>G GRCh38
NC_000008.10:g.19809355A>G , CM000670.1:g.19809355A>G GRCh37
NC_000008.9:g.19853635A>G NCBI36
NG_008855.1:g.17774A>G
NG_008855.2:g.55128A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.325A>G MANE Select ENSP00000497642.1:p.Ile109Val
ENST00000311322.8:c.325A>G ENSP00000309757.6:p.Ile109Val
ENST00000520959.5:c.97A>G ENSP00000428496.1:p.Ile33Val
ENST00000524029.5:c.325A>G ENSP00000428237.1:p.Ile109Val
NM_000237.2:c.325A>G NP_000228.1:p.Ile109Val
NM_000237.3:c.325A>G MANE Select NP_000228.1:p.Ile109Val
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