Canonical Allele Identifier: CA173379030
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1036422062
gnomAD v3: 8-19957767-G-T
gnomAD v4: 8-19957767-G-T
MyVariant Identifiers: chr8:g.19815278G>T (hg19) chr8:g.19957767G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957767G>T , CM000670.2:g.19957767G>T GRCh38
NC_000008.10:g.19815278G>T , CM000670.1:g.19815278G>T GRCh37
NC_000008.9:g.19859558G>T NCBI36
NG_008855.1:g.23697G>T
NG_008855.2:g.61051G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1493G>T MANE Select ENSP00000497642.1:n.1019-1493G>T
ENST00000650478.1:c.79+1684G>T ENSP00000497560.1:n.79+1684G>T
ENST00000311322.8:c.1019-1493G>T ENSP00000309757.6:n.1019-1493G>T
NM_000237.2:c.1019-1493G>T NP_000228.1:n.1019-1493G>T
NM_000237.3:c.1019-1493G>T MANE Select NP_000228.1:n.1019-1493G>T
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