Canonical Allele Identifier: CA459879385
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811686T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954175T>A , CM000670.2:g.19954175T>A GRCh38
NC_000008.10:g.19811686T>A , CM000670.1:g.19811686T>A GRCh37
NC_000008.9:g.19855966T>A NCBI36
NG_008855.1:g.20105T>A
NG_008855.2:g.57459T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.597T>A MANE Select ENSP00000497642.1:p.Ser199=
ENST00000311322.8:c.597T>A ENSP00000309757.6:p.Ser199=
NM_000237.2:c.597T>A NP_000228.1:p.Ser199=
NM_000237.3:c.597T>A MANE Select NP_000228.1:p.Ser199=