Canonical Allele Identifier: CA370469015
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19955882-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955882C>G , CM000670.2:g.19955882C>G GRCh38
NC_000008.10:g.19813393C>G , CM000670.1:g.19813393C>G GRCh37
NC_000008.9:g.19857673C>G NCBI36
NG_008855.1:g.21812C>G
NG_008855.2:g.59166C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.817C>G MANE Select ENSP00000497642.1:p.His273Asp
ENST00000311322.8:c.817C>G ENSP00000309757.6:p.His273Asp
NM_000237.2:c.817C>G NP_000228.1:p.His273Asp
NM_000237.3:c.817C>G MANE Select NP_000228.1:p.His273Asp