Canonical Allele Identifier: CA1769101607
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069960143

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953997G>T , CM000670.2:g.19953997G>T GRCh38
NC_000008.10:g.19811508G>T , CM000670.1:g.19811508G>T GRCh37
NC_000008.9:g.19855788G>T NCBI36
NG_008855.1:g.19927G>T
NG_008855.2:g.57281G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-123G>T MANE Select ENSP00000497642.1:n.542-123G>T
ENST00000311322.8:c.542-123G>T ENSP00000309757.6:n.542-123G>T
ENST00000520959.5:c.314-123G>T ENSP00000428496.1:n.314-123G>T
NM_000237.2:c.542-123G>T NP_000228.1:n.542-123G>T
NM_000237.3:c.542-123G>T MANE Select NP_000228.1:n.542-123G>T