Canonical Allele Identifier: CA4655367
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs182593459
ExAC: 8:19809284 C / G
gnomAD v2: 8-19809284-C-G
gnomAD v3: 8-19951773-C-G
gnomAD v4: 8-19951773-C-G
MyVariant Identifiers: chr8:g.19809284C>G (hg19) chr8:g.19951773C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951773C>G , CM000670.2:g.19951773C>G GRCh38
NC_000008.10:g.19809284C>G , CM000670.1:g.19809284C>G GRCh37
NC_000008.9:g.19853564C>G NCBI36
NG_008855.1:g.17703C>G
NG_008855.2:g.55057C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.254C>G MANE Select ENSP00000497642.1:p.Thr85Arg
ENST00000311322.8:c.254C>G ENSP00000309757.6:p.Thr85Arg
ENST00000520959.5:c.26C>G ENSP00000428496.1:p.Thr9Arg
ENST00000521994.1:n.511C>G
ENST00000522701.5:c.254C>G ENSP00000428557.1:p.Thr85Arg
ENST00000524029.5:c.254C>G ENSP00000428237.1:p.Thr85Arg
NM_000237.2:c.254C>G NP_000228.1:p.Thr85Arg
NM_000237.3:c.254C>G MANE Select NP_000228.1:p.Thr85Arg
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Search 100 bp 3'