Canonical Allele Identifier: CA1769107197
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070003004
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958046G>T , CM000670.2:g.19958046G>T GRCh38
NC_000008.10:g.19815557G>T , CM000670.1:g.19815557G>T GRCh37
NC_000008.9:g.19859837G>T NCBI36
NG_008855.1:g.23976G>T
NG_008855.2:g.61330G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1214G>T MANE Select ENSP00000497642.1:n.1019-1214G>T
ENST00000650478.1:c.79+1963G>T ENSP00000497560.1:n.79+1963G>T
ENST00000311322.8:c.1019-1214G>T ENSP00000309757.6:n.1019-1214G>T
NM_000237.2:c.1019-1214G>T NP_000228.1:n.1019-1214G>T
NM_000237.3:c.1019-1214G>T MANE Select NP_000228.1:n.1019-1214G>T
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