Canonical Allele Identifier: CA849560004
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1433274714
gnomAD v3: 8-19955528-A-C
gnomAD v4: 8-19955528-A-C
MyVariant Identifiers: chr8:g.19813039A>C (hg19) chr8:g.19955528A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955528A>C , CM000670.2:g.19955528A>C GRCh38
NC_000008.10:g.19813039A>C , CM000670.1:g.19813039A>C GRCh37
NC_000008.9:g.19857319A>C NCBI36
NG_008855.1:g.21458A>C
NG_008855.2:g.58812A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-313A>C MANE Select ENSP00000497642.1:n.776-313A>C
ENST00000311322.8:c.776-313A>C ENSP00000309757.6:n.776-313A>C
NM_000237.2:c.776-313A>C NP_000228.1:n.776-313A>C
NM_000237.3:c.776-313A>C MANE Select NP_000228.1:n.776-313A>C
Search 100 bp 5'
Search 100 bp 3'