Canonical Allele Identifier: CA459879341
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811665A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954154A>G , CM000670.2:g.19954154A>G GRCh38
NC_000008.10:g.19811665A>G , CM000670.1:g.19811665A>G GRCh37
NC_000008.9:g.19855945A>G NCBI36
NG_008855.1:g.20084A>G
NG_008855.2:g.57438A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.576A>G MANE Select ENSP00000497642.1:p.Ala192=
ENST00000311322.8:c.576A>G ENSP00000309757.6:p.Ala192=
NM_000237.2:c.576A>G NP_000228.1:p.Ala192=
NM_000237.3:c.576A>G MANE Select NP_000228.1:p.Ala192=
Search 100 bp 5'
Search 100 bp 3'