Canonical Allele Identifier: CA173378863
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1026798694
MyVariant Identifiers: chr8:g.19957337C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957337C>G , CM000670.2:g.19957337C>G GRCh38
NC_000008.10:g.19814848C>G , CM000670.1:g.19814848C>G GRCh37
NC_000008.9:g.19859128C>G NCBI36
NG_008855.1:g.23267C>G
NG_008855.2:g.60621C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1018+1254C>G MANE Select ENSP00000497642.1:n.1018+1254C>G
ENST00000650478.1:c.79+1254C>G ENSP00000497560.1:n.79+1254C>G
ENST00000311322.8:c.1018+1254C>G ENSP00000309757.6:n.1018+1254C>G
NM_000237.2:c.1018+1254C>G NP_000228.1:n.1018+1254C>G
NM_000237.3:c.1018+1254C>G MANE Select NP_000228.1:n.1018+1254C>G