Canonical Allele Identifier: CA173377711
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs965854267
gnomAD v2: 8-19812003-T-C
gnomAD v3: 8-19954492-T-C
gnomAD v4: 8-19954492-T-C
MyVariant Identifiers: chr8:g.19812003T>C (hg19) chr8:g.19954492T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954492T>C , CM000670.2:g.19954492T>C GRCh38
NC_000008.10:g.19812003T>C , CM000670.1:g.19812003T>C GRCh37
NC_000008.9:g.19856283T>C NCBI36
NG_008855.1:g.20422T>C
NG_008855.2:g.57776T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+139T>C MANE Select ENSP00000497642.1:n.775+139T>C
ENST00000311322.8:c.775+139T>C ENSP00000309757.6:n.775+139T>C
NM_000237.2:c.775+139T>C NP_000228.1:n.775+139T>C
NM_000237.3:c.775+139T>C MANE Select NP_000228.1:n.775+139T>C
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