Canonical Allele Identifier: CA459879469
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811740T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954229T>G , CM000670.2:g.19954229T>G GRCh38
NC_000008.10:g.19811740T>G , CM000670.1:g.19811740T>G GRCh37
NC_000008.9:g.19856020T>G NCBI36
NG_008855.1:g.20159T>G
NG_008855.2:g.57513T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.651T>G MANE Select ENSP00000497642.1:p.Pro217=
ENST00000311322.8:c.651T>G ENSP00000309757.6:p.Pro217=
NM_000237.2:c.651T>G NP_000228.1:p.Pro217=
NM_000237.3:c.651T>G MANE Select NP_000228.1:p.Pro217=