Canonical Allele Identifier: CA1769111708
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070042095
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961888G>A , CM000670.2:g.19961888G>A GRCh38
NC_000008.10:g.19819399G>A , CM000670.1:g.19819399G>A GRCh37
NC_000008.9:g.19863679G>A NCBI36
NG_008855.1:g.27818G>A
NG_008855.2:g.65172G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1323-227G>A MANE Select ENSP00000497642.1:n.1323-227G>A
ENST00000650478.1:c.263-227G>A ENSP00000497560.1:n.263-227G>A
ENST00000311322.8:c.1323-227G>A ENSP00000309757.6:n.1323-227G>A
NM_000237.2:c.1323-227G>A NP_000228.1:n.1323-227G>A
NM_000237.3:c.1323-227G>A MANE Select NP_000228.1:n.1323-227G>A
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