Canonical Allele Identifier: CA1769104270
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs559329520
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955638C>G , CM000670.2:g.19955638C>G GRCh38
NC_000008.10:g.19813149C>G , CM000670.1:g.19813149C>G GRCh37
NC_000008.9:g.19857429C>G NCBI36
NG_008855.1:g.21568C>G
NG_008855.2:g.58922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-203C>G MANE Select ENSP00000497642.1:n.776-203C>G
ENST00000311322.8:c.776-203C>G ENSP00000309757.6:n.776-203C>G
NM_000237.2:c.776-203C>G NP_000228.1:n.776-203C>G
NM_000237.3:c.776-203C>G MANE Select NP_000228.1:n.776-203C>G
Search 100 bp 5'
Search 100 bp 3'