Canonical Allele Identifier: CA173378908
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1011551408
gnomAD v2: 8-19815002-T-C
gnomAD v3: 8-19957491-T-C
gnomAD v4: 8-19957491-T-C
MyVariant Identifiers: chr8:g.19815002T>C (hg19) chr8:g.19957491T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957491T>C , CM000670.2:g.19957491T>C GRCh38
NC_000008.10:g.19815002T>C , CM000670.1:g.19815002T>C GRCh37
NC_000008.9:g.19859282T>C NCBI36
NG_008855.1:g.23421T>C
NG_008855.2:g.60775T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1408T>C MANE Select ENSP00000497642.1:n.1018+1408T>C
ENST00000650478.1:c.79+1408T>C ENSP00000497560.1:n.79+1408T>C
ENST00000311322.8:c.1018+1408T>C ENSP00000309757.6:n.1018+1408T>C
NM_000237.2:c.1018+1408T>C NP_000228.1:n.1018+1408T>C
NM_000237.3:c.1018+1408T>C MANE Select NP_000228.1:n.1018+1408T>C
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