Canonical Allele Identifier: CA459879354
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811671C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954160C>G , CM000670.2:g.19954160C>G GRCh38
NC_000008.10:g.19811671C>G , CM000670.1:g.19811671C>G GRCh37
NC_000008.9:g.19855951C>G NCBI36
NG_008855.1:g.20090C>G
NG_008855.2:g.57444C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.582C>G MANE Select ENSP00000497642.1:p.Ala194=
ENST00000311322.8:c.582C>G ENSP00000309757.6:p.Ala194=
NM_000237.2:c.582C>G NP_000228.1:p.Ala194=
NM_000237.3:c.582C>G MANE Select NP_000228.1:p.Ala194=
Search 100 bp 5'
Search 100 bp 3'