Canonical Allele Identifier: CA1111552289
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069978140
gnomAD v3: 8-19955706-A-G
gnomAD v4: 8-19955706-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955706A>G , CM000670.2:g.19955706A>G GRCh38
NC_000008.10:g.19813217A>G , CM000670.1:g.19813217A>G GRCh37
NC_000008.9:g.19857497A>G NCBI36
NG_008855.1:g.21636A>G
NG_008855.2:g.58990A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-135A>G MANE Select ENSP00000497642.1:n.776-135A>G
ENST00000311322.8:c.776-135A>G ENSP00000309757.6:n.776-135A>G
NM_000237.2:c.776-135A>G NP_000228.1:n.776-135A>G
NM_000237.3:c.776-135A>G MANE Select NP_000228.1:n.776-135A>G