Canonical Allele Identifier: CA849568003
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs562346489
gnomAD v3: 8-19966970-G-C
gnomAD v4: 8-19966970-G-C
MyVariant Identifiers: chr8:g.19824481G>C (hg19) chr8:g.19966970G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966970G>C , CM000670.2:g.19966970G>C GRCh38
NC_000008.10:g.19824481G>C , CM000670.1:g.19824481G>C GRCh37
NC_000008.9:g.19868761G>C NCBI36
NG_008855.1:g.32900G>C
NG_008855.2:g.70254G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1660G>C MANE Select ENSP00000497642.1:n.*1660G>C
ENST00000650478.1:c.2028G>C ENSP00000497560.1:n.2028G>C
ENST00000311322.8:c.*1660G>C ENSP00000309757.6:n.*1660G>C
NM_000237.2:c.*1660G>C NP_000228.1:n.*1660G>C
NM_000237.3:c.*1660G>C MANE Select NP_000228.1:n.*1660G>C
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