Canonical Allele Identifier: CA370469249
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813497G>C (hg19) chr8:g.19955986G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955986G>C , CM000670.2:g.19955986G>C GRCh38
NC_000008.10:g.19813497G>C , CM000670.1:g.19813497G>C GRCh37
NC_000008.9:g.19857777G>C NCBI36
NG_008855.1:g.21916G>C
NG_008855.2:g.59270G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.921G>C MANE Select ENSP00000497642.1:p.Lys307Asn
ENST00000311322.8:c.921G>C ENSP00000309757.6:p.Lys307Asn
NM_000237.2:c.921G>C NP_000228.1:p.Lys307Asn
NM_000237.3:c.921G>C MANE Select NP_000228.1:p.Lys307Asn
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