Canonical Allele Identifier: CA173378984
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs947639775
MyVariant Identifiers: chr8:g.19815143C>A (hg19) chr8:g.19957632C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957632C>A , CM000670.2:g.19957632C>A GRCh38
NC_000008.10:g.19815143C>A , CM000670.1:g.19815143C>A GRCh37
NC_000008.9:g.19859423C>A NCBI36
NG_008855.1:g.23562C>A
NG_008855.2:g.60916C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1549C>A MANE Select ENSP00000497642.1:n.1018+1549C>A
ENST00000650478.1:c.79+1549C>A ENSP00000497560.1:n.79+1549C>A
ENST00000311322.8:c.1018+1549C>A ENSP00000309757.6:n.1018+1549C>A
NM_000237.2:c.1018+1549C>A NP_000228.1:n.1018+1549C>A
NM_000237.3:c.1018+1549C>A MANE Select NP_000228.1:n.1018+1549C>A
Search 100 bp 5'
Search 100 bp 3'