Canonical Allele Identifier: CA1769106523
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069996197

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957495G>C , CM000670.2:g.19957495G>C GRCh38
NC_000008.10:g.19815006G>C , CM000670.1:g.19815006G>C GRCh37
NC_000008.9:g.19859286G>C NCBI36
NG_008855.1:g.23425G>C
NG_008855.2:g.60779G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1412G>C MANE Select ENSP00000497642.1:n.1018+1412G>C
ENST00000650478.1:c.79+1412G>C ENSP00000497560.1:n.79+1412G>C
ENST00000311322.8:c.1018+1412G>C ENSP00000309757.6:n.1018+1412G>C
NM_000237.2:c.1018+1412G>C NP_000228.1:n.1018+1412G>C
NM_000237.3:c.1018+1412G>C MANE Select NP_000228.1:n.1018+1412G>C