Canonical Allele Identifier: CA4655488
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs757546424
gnomAD v2: 8-19811747-A-C
gnomAD v4: 8-19954236-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954236A>C , CM000670.2:g.19954236A>C GRCh38
NC_000008.10:g.19811747A>C , CM000670.1:g.19811747A>C GRCh37
NC_000008.9:g.19856027A>C NCBI36
NG_008855.1:g.20166A>C
NG_008855.2:g.57520A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.658A>C MANE Select ENSP00000497642.1:p.Ser220Arg
ENST00000311322.8:c.658A>C ENSP00000309757.6:p.Ser220Arg
NM_000237.2:c.658A>C NP_000228.1:p.Ser220Arg
NM_000237.3:c.658A>C MANE Select NP_000228.1:p.Ser220Arg