Canonical Allele Identifier: CA173378126
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1029371564
MyVariant Identifiers: chr8:g.19813143A>G (hg19) chr8:g.19955632A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955632A>G , CM000670.2:g.19955632A>G GRCh38
NC_000008.10:g.19813143A>G , CM000670.1:g.19813143A>G GRCh37
NC_000008.9:g.19857423A>G NCBI36
NG_008855.1:g.21562A>G
NG_008855.2:g.58916A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-209A>G MANE Select ENSP00000497642.1:n.776-209A>G
ENST00000311322.8:c.776-209A>G ENSP00000309757.6:n.776-209A>G
NM_000237.2:c.776-209A>G NP_000228.1:n.776-209A>G
NM_000237.3:c.776-209A>G MANE Select NP_000228.1:n.776-209A>G
Search 100 bp 5'
Search 100 bp 3'