Canonical Allele Identifier: CA849565347
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs986201398
MyVariant Identifiers: chr8:g.19820237C>A (hg19) chr8:g.19962726C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962726C>A , CM000670.2:g.19962726C>A GRCh38
NC_000008.10:g.19820237C>A , CM000670.1:g.19820237C>A GRCh37
NC_000008.9:g.19864517C>A NCBI36
NG_008855.1:g.28656C>A
NG_008855.2:g.66010C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1427+507C>A MANE Select ENSP00000497642.1:n.1427+507C>A
ENST00000650478.1:c.367+507C>A ENSP00000497560.1:n.367+507C>A
ENST00000311322.8:c.1427+507C>A ENSP00000309757.6:n.1427+507C>A
NM_000237.2:c.1427+507C>A NP_000228.1:n.1427+507C>A
NM_000237.3:c.1427+507C>A MANE Select NP_000228.1:n.1427+507C>A
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