Canonical Allele Identifier: CA1111552224
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1401917486
gnomAD v3: 8-19955530-G-T
gnomAD v4: 8-19955530-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955530G>T , CM000670.2:g.19955530G>T GRCh38
NC_000008.10:g.19813041G>T , CM000670.1:g.19813041G>T GRCh37
NC_000008.9:g.19857321G>T NCBI36
NG_008855.1:g.21460G>T
NG_008855.2:g.58814G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-311G>T MANE Select ENSP00000497642.1:n.776-311G>T
ENST00000311322.8:c.776-311G>T ENSP00000309757.6:n.776-311G>T
NM_000237.2:c.776-311G>T NP_000228.1:n.776-311G>T
NM_000237.3:c.776-311G>T MANE Select NP_000228.1:n.776-311G>T
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