Canonical Allele Identifier: CA370467716
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809430G>C (hg19) chr8:g.19951919G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951919G>C , CM000670.2:g.19951919G>C GRCh38
NC_000008.10:g.19809430G>C , CM000670.1:g.19809430G>C GRCh37
NC_000008.9:g.19853710G>C NCBI36
NG_008855.1:g.17849G>C
NG_008855.2:g.55203G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.400G>C MANE Select ENSP00000497642.1:p.Asp134His
ENST00000311322.8:c.400G>C ENSP00000309757.6:p.Asp134His
ENST00000520959.5:c.172G>C ENSP00000428496.1:p.Asp58His
NM_000237.2:c.400G>C NP_000228.1:p.Asp134His
NM_000237.3:c.400G>C MANE Select NP_000228.1:p.Asp134His
Search 100 bp 5'
Search 100 bp 3'