Canonical Allele Identifier: CA4655566
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs764867247
gnomAD v2: 8-19813552-A-G
gnomAD v4: 8-19956041-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956041A>G , CM000670.2:g.19956041A>G GRCh38
NC_000008.10:g.19813552A>G , CM000670.1:g.19813552A>G GRCh37
NC_000008.9:g.19857832A>G NCBI36
NG_008855.1:g.21971A>G
NG_008855.2:g.59325A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.976A>G MANE Select ENSP00000497642.1:p.Ser326Gly
ENST00000650478.1:c.37A>G ENSP00000497560.1:p.Ser13Gly
ENST00000311322.8:c.976A>G ENSP00000309757.6:p.Ser326Gly
NM_000237.2:c.976A>G NP_000228.1:p.Ser326Gly
NM_000237.3:c.976A>G MANE Select NP_000228.1:p.Ser326Gly