Canonical Allele Identifier: CA459879479
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811752T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954241T>C , CM000670.2:g.19954241T>C GRCh38
NC_000008.10:g.19811752T>C , CM000670.1:g.19811752T>C GRCh37
NC_000008.9:g.19856032T>C NCBI36
NG_008855.1:g.20171T>C
NG_008855.2:g.57525T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.663T>C MANE Select ENSP00000497642.1:p.Ile221=
ENST00000311322.8:c.663T>C ENSP00000309757.6:p.Ile221=
NM_000237.2:c.663T>C NP_000228.1:p.Ile221=
NM_000237.3:c.663T>C MANE Select NP_000228.1:p.Ile221=