Canonical Allele Identifier: CA459879464
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs756420241
gnomAD v3: 8-19954223-G-T
gnomAD v4: 8-19954223-G-T
MyVariant Identifiers: chr8:g.19811734G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954223G>T , CM000670.2:g.19954223G>T GRCh38
NC_000008.10:g.19811734G>T , CM000670.1:g.19811734G>T GRCh37
NC_000008.9:g.19856014G>T NCBI36
NG_008855.1:g.20153G>T
NG_008855.2:g.57507G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.645G>T MANE Select ENSP00000497642.1:p.Gly215=
ENST00000311322.8:c.645G>T ENSP00000309757.6:p.Gly215=
NM_000237.2:c.645G>T NP_000228.1:p.Gly215=
NM_000237.3:c.645G>T MANE Select NP_000228.1:p.Gly215=