Canonical Allele Identifier: CA1769103256
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1259276377
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954623C>A , CM000670.2:g.19954623C>A GRCh38
NC_000008.10:g.19812134C>A , CM000670.1:g.19812134C>A GRCh37
NC_000008.9:g.19856414C>A NCBI36
NG_008855.1:g.20553C>A
NG_008855.2:g.57907C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+270C>A MANE Select ENSP00000497642.1:n.775+270C>A
ENST00000311322.8:c.775+270C>A ENSP00000309757.6:n.775+270C>A
NM_000237.2:c.775+270C>A NP_000228.1:n.775+270C>A
NM_000237.3:c.775+270C>A MANE Select NP_000228.1:n.775+270C>A
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