Canonical Allele Identifier: CA4655525
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs758756700
gnomAD v2: 8-19813305-T-A
gnomAD v3: 8-19955794-T-A
gnomAD v4: 8-19955794-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955794T>A , CM000670.2:g.19955794T>A GRCh38
NC_000008.10:g.19813305T>A , CM000670.1:g.19813305T>A GRCh37
NC_000008.9:g.19857585T>A NCBI36
NG_008855.1:g.21724T>A
NG_008855.2:g.59078T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-47T>A MANE Select ENSP00000497642.1:n.776-47T>A
ENST00000311322.8:c.776-47T>A ENSP00000309757.6:n.776-47T>A
NM_000237.2:c.776-47T>A NP_000228.1:n.776-47T>A
NM_000237.3:c.776-47T>A MANE Select NP_000228.1:n.776-47T>A