Canonical Allele Identifier: CA849557665
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1192859974
MyVariant Identifiers: chr8:g.19809645G>C (hg19) chr8:g.19952134G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952134G>C , CM000670.2:g.19952134G>C GRCh38
NC_000008.10:g.19809645G>C , CM000670.1:g.19809645G>C GRCh37
NC_000008.9:g.19853925G>C NCBI36
NG_008855.1:g.18064G>C
NG_008855.2:g.55418G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+186G>C MANE Select ENSP00000497642.1:n.429+186G>C
ENST00000311322.8:c.429+186G>C ENSP00000309757.6:n.429+186G>C
ENST00000520959.5:c.201+186G>C ENSP00000428496.1:n.201+186G>C
NM_000237.2:c.429+186G>C NP_000228.1:n.429+186G>C
NM_000237.3:c.429+186G>C MANE Select NP_000228.1:n.429+186G>C
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