Canonical Allele Identifier: CA173618732
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs991431728
gnomAD v3: 8-19966781-G-A
gnomAD v4: 8-19966781-G-A
MyVariant Identifiers: chr8:g.19824292G>A (hg19) chr8:g.19966781G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966781G>A , CM000670.2:g.19966781G>A GRCh38
NC_000008.10:g.19824292G>A , CM000670.1:g.19824292G>A GRCh37
NC_000008.9:g.19868572G>A NCBI36
NG_008855.1:g.32711G>A
NG_008855.2:g.70065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1471G>A MANE Select ENSP00000497642.1:n.*1471G>A
ENST00000650478.1:c.1839G>A ENSP00000497560.1:n.1839G>A
ENST00000311322.8:c.*1471G>A ENSP00000309757.6:n.*1471G>A
NM_000237.2:c.*1471G>A NP_000228.1:n.*1471G>A
NM_000237.3:c.*1471G>A MANE Select NP_000228.1:n.*1471G>A
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