Canonical Allele Identifier: CA4655652
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs755257326
ExAC: 8:19818384 T / G
gnomAD v2: 8-19818384-T-G
gnomAD v3: 8-19960873-T-G
gnomAD v4: 8-19960873-T-G
MyVariant Identifiers: chr8:g.19818384T>G (hg19) chr8:g.19960873T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960873T>G , CM000670.2:g.19960873T>G GRCh38
NC_000008.10:g.19818384T>G , CM000670.1:g.19818384T>G GRCh37
NC_000008.9:g.19862664T>G NCBI36
NG_008855.1:g.26803T>G
NG_008855.2:g.64157T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-28T>G MANE Select ENSP00000497642.1:n.1140-28T>G
ENST00000650478.1:c.80-28T>G ENSP00000497560.1:n.80-28T>G
ENST00000311322.8:c.1140-28T>G ENSP00000309757.6:n.1140-28T>G
NM_000237.2:c.1140-28T>G NP_000228.1:n.1140-28T>G
NM_000237.3:c.1140-28T>G MANE Select NP_000228.1:n.1140-28T>G
Search 100 bp 5'
Search 100 bp 3'