Canonical Allele Identifier: CA580502364
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1541553
ClinVar RCV Id: RCV002157455
dbSNP Id: rs1385911121
gnomAD v2: 8-19813348-C-T
gnomAD v4: 8-19955837-C-T
MyVariant Identifiers: chr8:g.19813348C>T (hg19) chr8:g.19955837C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955837C>T , CM000670.2:g.19955837C>T GRCh38
NC_000008.10:g.19813348C>T , CM000670.1:g.19813348C>T GRCh37
NC_000008.9:g.19857628C>T NCBI36
NG_008855.1:g.21767C>T
NG_008855.2:g.59121C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-4C>T MANE Select ENSP00000497642.1:n.776-4C>T
ENST00000311322.8:c.776-4C>T ENSP00000309757.6:n.776-4C>T
NM_000237.2:c.776-4C>T NP_000228.1:n.776-4C>T
NM_000237.3:c.776-4C>T MANE Select NP_000228.1:n.776-4C>T
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