Canonical Allele Identifier: CA4655459
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs550087990
gnomAD v2: 8-19811607-G-T
gnomAD v3: 8-19954096-G-T
gnomAD v4: 8-19954096-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954096G>T , CM000670.2:g.19954096G>T GRCh38
NC_000008.10:g.19811607G>T , CM000670.1:g.19811607G>T GRCh37
NC_000008.9:g.19855887G>T NCBI36
NG_008855.1:g.20026G>T
NG_008855.2:g.57380G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-24G>T MANE Select ENSP00000497642.1:n.542-24G>T
ENST00000311322.8:c.542-24G>T ENSP00000309757.6:n.542-24G>T
ENST00000520959.5:c.314-24G>T ENSP00000428496.1:n.314-24G>T
NM_000237.2:c.542-24G>T NP_000228.1:n.542-24G>T
NM_000237.3:c.542-24G>T MANE Select NP_000228.1:n.542-24G>T