Canonical Allele Identifier: CA849549613
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs961858458
MyVariant Identifiers: chr8:g.19796828C>G (hg19) chr8:g.19939317C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939317C>G , CM000670.2:g.19939317C>G GRCh38
NC_000008.10:g.19796828C>G , CM000670.1:g.19796828C>G GRCh37
NC_000008.9:g.19841108C>G NCBI36
NG_008855.1:g.5247C>G
NG_008855.2:g.42601C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-124C>G MANE Select ENSP00000497642.1:n.-124C>G
ENST00000311322.8:c.-124C>G ENSP00000309757.6:n.-124C>G
ENST00000519773.1:c.-124C>G ENSP00000431028.1:n.-124C>G
ENST00000520959.5:c.-140-8863C>G ENSP00000428496.1:n.-140-8863C>G
ENST00000521994.1:n.62C>G
ENST00000522701.5:c.-124C>G ENSP00000428557.1:n.-124C>G
ENST00000524029.5:c.-124C>G ENSP00000428237.1:n.-124C>G
NM_000237.2:c.-124C>G NP_000228.1:n.-124C>G
NM_000237.3:c.-124C>G MANE Select NP_000228.1:n.-124C>G
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