Canonical Allele Identifier: CA173376511
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs373932223
gnomAD v2: 8-19809627-A-T
gnomAD v3: 8-19952116-A-T
gnomAD v4: 8-19952116-A-T
MyVariant Identifiers: chr8:g.19809627A>T (hg19) chr8:g.19952116A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952116A>T , CM000670.2:g.19952116A>T GRCh38
NC_000008.10:g.19809627A>T , CM000670.1:g.19809627A>T GRCh37
NC_000008.9:g.19853907A>T NCBI36
NG_008855.1:g.18046A>T
NG_008855.2:g.55400A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+168A>T MANE Select ENSP00000497642.1:n.429+168A>T
ENST00000311322.8:c.429+168A>T ENSP00000309757.6:n.429+168A>T
ENST00000520959.5:c.201+168A>T ENSP00000428496.1:n.201+168A>T
NM_000237.2:c.429+168A>T NP_000228.1:n.429+168A>T
NM_000237.3:c.429+168A>T MANE Select NP_000228.1:n.429+168A>T
Search 100 bp 5'
Search 100 bp 3'