Canonical Allele Identifier: CA370469291
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813516G>C (hg19) chr8:g.19956005G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956005G>C , CM000670.2:g.19956005G>C GRCh38
NC_000008.10:g.19813516G>C , CM000670.1:g.19813516G>C GRCh37
NC_000008.9:g.19857796G>C NCBI36
NG_008855.1:g.21935G>C
NG_008855.2:g.59289G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.940G>C MANE Select ENSP00000497642.1:p.Gly314Arg
ENST00000650478.1:c.1G>C ENSP00000497560.1:p.Gly1Arg
ENST00000311322.8:c.940G>C ENSP00000309757.6:p.Gly314Arg
NM_000237.2:c.940G>C NP_000228.1:p.Gly314Arg
NM_000237.3:c.940G>C MANE Select NP_000228.1:p.Gly314Arg
Search 100 bp 5'
Search 100 bp 3'