Canonical Allele Identifier: CA173618756
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs994279533
gnomAD v3: 8-19966966-C-T
gnomAD v4: 8-19966966-C-T
MyVariant Identifiers: chr8:g.19824477C>T (hg19) chr8:g.19966966C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966966C>T , CM000670.2:g.19966966C>T GRCh38
NC_000008.10:g.19824477C>T , CM000670.1:g.19824477C>T GRCh37
NC_000008.9:g.19868757C>T NCBI36
NG_008855.1:g.32896C>T
NG_008855.2:g.70250C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1656C>T MANE Select ENSP00000497642.1:n.*1656C>T
ENST00000650478.1:c.2024C>T ENSP00000497560.1:n.2024C>T
ENST00000311322.8:c.*1656C>T ENSP00000309757.6:n.*1656C>T
NM_000237.2:c.*1656C>T NP_000228.1:n.*1656C>T
NM_000237.3:c.*1656C>T MANE Select NP_000228.1:n.*1656C>T
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