Canonical Allele Identifier: CA370468754
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1339509016
gnomAD v2: 8-19811849-G-A
gnomAD v4: 8-19954338-G-A
MyVariant Identifiers: chr8:g.19811849G>A (hg19) chr8:g.19954338G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954338G>A , CM000670.2:g.19954338G>A GRCh38
NC_000008.10:g.19811849G>A , CM000670.1:g.19811849G>A GRCh37
NC_000008.9:g.19856129G>A NCBI36
NG_008855.1:g.20268G>A
NG_008855.2:g.57622G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.760G>A MANE Select ENSP00000497642.1:p.Glu254Lys
ENST00000311322.8:c.760G>A ENSP00000309757.6:p.Glu254Lys
NM_000237.2:c.760G>A NP_000228.1:p.Glu254Lys
NM_000237.3:c.760G>A MANE Select NP_000228.1:p.Glu254Lys
Search 100 bp 5'
Search 100 bp 3'