Canonical Allele Identifier: CA459879281
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811632C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954121C>G , CM000670.2:g.19954121C>G GRCh38
NC_000008.10:g.19811632C>G , CM000670.1:g.19811632C>G GRCh37
NC_000008.9:g.19855912C>G NCBI36
NG_008855.1:g.20051C>G
NG_008855.2:g.57405C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.543C>G MANE Select ENSP00000497642.1:p.Gly181=
ENST00000311322.8:c.543C>G ENSP00000309757.6:p.Gly181=
ENST00000520959.5:c.315C>G ENSP00000428496.1:p.Gly105=
NM_000237.2:c.543C>G NP_000228.1:p.Gly181=
NM_000237.3:c.543C>G MANE Select NP_000228.1:p.Gly181=