Canonical Allele Identifier: CA849556872
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1259409806
MyVariant Identifiers: chr8:g.19809034G>A (hg19) chr8:g.19951523G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951523G>A , CM000670.2:g.19951523G>A GRCh38
NC_000008.10:g.19809034G>A , CM000670.1:g.19809034G>A GRCh37
NC_000008.9:g.19853314G>A NCBI36
NG_008855.1:g.17453G>A
NG_008855.2:g.54807G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-246G>A MANE Select ENSP00000497642.1:n.250-246G>A
ENST00000311322.8:c.250-246G>A ENSP00000309757.6:n.250-246G>A
ENST00000520959.5:c.22-246G>A ENSP00000428496.1:n.22-246G>A
ENST00000521994.1:n.435-174G>A
ENST00000522701.5:c.250-246G>A ENSP00000428557.1:n.250-246G>A
ENST00000524029.5:c.250-246G>A ENSP00000428237.1:n.250-246G>A
NM_000237.2:c.250-246G>A NP_000228.1:n.250-246G>A
NM_000237.3:c.250-246G>A MANE Select NP_000228.1:n.250-246G>A
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