Canonical Allele Identifier: CA849561528
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1440746603
gnomAD v3: 8-19957728-A-T
gnomAD v4: 8-19957728-A-T
MyVariant Identifiers: chr8:g.19815239A>T (hg19) chr8:g.19957728A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957728A>T , CM000670.2:g.19957728A>T GRCh38
NC_000008.10:g.19815239A>T , CM000670.1:g.19815239A>T GRCh37
NC_000008.9:g.19859519A>T NCBI36
NG_008855.1:g.23658A>T
NG_008855.2:g.61012A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1532A>T MANE Select ENSP00000497642.1:n.1019-1532A>T
ENST00000650478.1:c.79+1645A>T ENSP00000497560.1:n.79+1645A>T
ENST00000311322.8:c.1019-1532A>T ENSP00000309757.6:n.1019-1532A>T
NM_000237.2:c.1019-1532A>T NP_000228.1:n.1019-1532A>T
NM_000237.3:c.1019-1532A>T MANE Select NP_000228.1:n.1019-1532A>T
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