Canonical Allele Identifier: CA173378093
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1001574113
gnomAD v2: 8-19813073-T-G
gnomAD v3: 8-19955562-T-G
gnomAD v4: 8-19955562-T-G
MyVariant Identifiers: chr8:g.19813073T>G (hg19) chr8:g.19955562T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955562T>G , CM000670.2:g.19955562T>G GRCh38
NC_000008.10:g.19813073T>G , CM000670.1:g.19813073T>G GRCh37
NC_000008.9:g.19857353T>G NCBI36
NG_008855.1:g.21492T>G
NG_008855.2:g.58846T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-279T>G MANE Select ENSP00000497642.1:n.776-279T>G
ENST00000311322.8:c.776-279T>G ENSP00000309757.6:n.776-279T>G
NM_000237.2:c.776-279T>G NP_000228.1:n.776-279T>G
NM_000237.3:c.776-279T>G MANE Select NP_000228.1:n.776-279T>G
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