Canonical Allele Identifier: CA370638614
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070032749
MyVariant Identifiers: chr8:g.19818460G>C (hg19) chr8:g.19960949G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960949G>C , CM000670.2:g.19960949G>C GRCh38
NC_000008.10:g.19818460G>C , CM000670.1:g.19818460G>C GRCh37
NC_000008.9:g.19862740G>C NCBI36
NG_008855.1:g.26879G>C
NG_008855.2:g.64233G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1188G>C MANE Select ENSP00000497642.1:p.Glu396Asp
ENST00000650478.1:c.128G>C ENSP00000497560.1:n.128G>C
ENST00000311322.8:c.1188G>C ENSP00000309757.6:p.Glu396Asp
NM_000237.2:c.1188G>C NP_000228.1:p.Glu396Asp
NM_000237.3:c.1188G>C MANE Select NP_000228.1:p.Glu396Asp
Search 100 bp 5'
Search 100 bp 3'