Canonical Allele Identifier: CA1769104290
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069977808
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955663T>C , CM000670.2:g.19955663T>C GRCh38
NC_000008.10:g.19813174T>C , CM000670.1:g.19813174T>C GRCh37
NC_000008.9:g.19857454T>C NCBI36
NG_008855.1:g.21593T>C
NG_008855.2:g.58947T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-178T>C MANE Select ENSP00000497642.1:n.776-178T>C
ENST00000311322.8:c.776-178T>C ENSP00000309757.6:n.776-178T>C
NM_000237.2:c.776-178T>C NP_000228.1:n.776-178T>C
NM_000237.3:c.776-178T>C MANE Select NP_000228.1:n.776-178T>C
Search 100 bp 5'
Search 100 bp 3'