Canonical Allele Identifier: CA459879422
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19955875-C-T
MyVariant Identifiers: chr8:g.19813386C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955875C>T , CM000670.2:g.19955875C>T GRCh38
NC_000008.10:g.19813386C>T , CM000670.1:g.19813386C>T GRCh37
NC_000008.9:g.19857666C>T NCBI36
NG_008855.1:g.21805C>T
NG_008855.2:g.59159C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.810C>T MANE Select ENSP00000497642.1:p.Arg270=
ENST00000311322.8:c.810C>T ENSP00000309757.6:p.Arg270=
NM_000237.2:c.810C>T NP_000228.1:p.Arg270=
NM_000237.3:c.810C>T MANE Select NP_000228.1:p.Arg270=