Canonical Allele Identifier: CA459879554
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811857A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954346A>T , CM000670.2:g.19954346A>T GRCh38
NC_000008.10:g.19811857A>T , CM000670.1:g.19811857A>T GRCh37
NC_000008.9:g.19856137A>T NCBI36
NG_008855.1:g.20276A>T
NG_008855.2:g.57630A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.768A>T MANE Select ENSP00000497642.1:p.Gly256=
ENST00000311322.8:c.768A>T ENSP00000309757.6:p.Gly256=
NM_000237.2:c.768A>T NP_000228.1:p.Gly256=
NM_000237.3:c.768A>T MANE Select NP_000228.1:p.Gly256=
Search 100 bp 5'
Search 100 bp 3'