Canonical Allele Identifier: CA1769101688
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069960449
gnomAD v4: 8-19954042-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954042A>C , CM000670.2:g.19954042A>C GRCh38
NC_000008.10:g.19811553A>C , CM000670.1:g.19811553A>C GRCh37
NC_000008.9:g.19855833A>C NCBI36
NG_008855.1:g.19972A>C
NG_008855.2:g.57326A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-78A>C MANE Select ENSP00000497642.1:n.542-78A>C
ENST00000311322.8:c.542-78A>C ENSP00000309757.6:n.542-78A>C
ENST00000520959.5:c.314-78A>C ENSP00000428496.1:n.314-78A>C
NM_000237.2:c.542-78A>C NP_000228.1:n.542-78A>C
NM_000237.3:c.542-78A>C MANE Select NP_000228.1:n.542-78A>C
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