Canonical Allele Identifier: CA580502360
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1217863204
gnomAD v2: 8-19813326-A-C
gnomAD v3: 8-19955815-A-C
gnomAD v4: 8-19955815-A-C
MyVariant Identifiers: chr8:g.19813326A>C (hg19) chr8:g.19955815A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955815A>C , CM000670.2:g.19955815A>C GRCh38
NC_000008.10:g.19813326A>C , CM000670.1:g.19813326A>C GRCh37
NC_000008.9:g.19857606A>C NCBI36
NG_008855.1:g.21745A>C
NG_008855.2:g.59099A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-26A>C MANE Select ENSP00000497642.1:n.776-26A>C
ENST00000311322.8:c.776-26A>C ENSP00000309757.6:n.776-26A>C
NM_000237.2:c.776-26A>C NP_000228.1:n.776-26A>C
NM_000237.3:c.776-26A>C MANE Select NP_000228.1:n.776-26A>C
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