Canonical Allele Identifier: CA459879466
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs140457997
MyVariant Identifiers: chr8:g.19811737C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954226C>A , CM000670.2:g.19954226C>A GRCh38
NC_000008.10:g.19811737C>A , CM000670.1:g.19811737C>A GRCh37
NC_000008.9:g.19856017C>A NCBI36
NG_008855.1:g.20156C>A
NG_008855.2:g.57510C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.648C>A MANE Select ENSP00000497642.1:p.Ser216=
ENST00000311322.8:c.648C>A ENSP00000309757.6:p.Ser216=
NM_000237.2:c.648C>A NP_000228.1:p.Ser216=
NM_000237.3:c.648C>A MANE Select NP_000228.1:p.Ser216=