Canonical Allele Identifier: CA2686362040
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19962050-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962050G>C , CM000670.2:g.19962050G>C GRCh38
NC_000008.10:g.19819561G>C , CM000670.1:g.19819561G>C GRCh37
NC_000008.9:g.19863841G>C NCBI36
NG_008855.1:g.27980G>C
NG_008855.2:g.65334G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-65G>C MANE Select ENSP00000497642.1:n.1323-65G>C
ENST00000650478.1:c.263-65G>C ENSP00000497560.1:n.263-65G>C
ENST00000311322.8:c.1323-65G>C ENSP00000309757.6:n.1323-65G>C
NM_000237.2:c.1323-65G>C NP_000228.1:n.1323-65G>C
NM_000237.3:c.1323-65G>C MANE Select NP_000228.1:n.1323-65G>C
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