Canonical Allele Identifier: CA4655529

Gene: LPL

Linked Data

• dbSNP Id: rs568292586
• ExAC: 8:19813311 T / C
• gnomAD v2: 8-19813311-T-C
• gnomAD v3: 8-19955800-T-C
• gnomAD v4: 8-19955800-T-C
• MyVariant Identifiers: chr8:g.19813311T>C (hg19) ; chr8:g.19955800T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19955800T>C , CM000670.2:g.19955800T>C	GRCh38
NC_000008.10:g.19813311T>C , CM000670.1:g.19813311T>C	GRCh37
NC_000008.9:g.19857591T>C	NCBI36
NG_008855.1:g.21730T>C
NG_008855.2:g.59084T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.776-41T>C MANE Select	ENSP00000497642.1:n.776-41T>C
ENST00000311322.8:c.776-41T>C	ENSP00000309757.6:n.776-41T>C
NM_000237.2:c.776-41T>C	NP_000228.1:n.776-41T>C
NM_000237.3:c.776-41T>C MANE Select	NP_000228.1:n.776-41T>C