Canonical Allele Identifier: CA370468611
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811804T>G (hg19) chr8:g.19954293T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954293T>G , CM000670.2:g.19954293T>G GRCh38
NC_000008.10:g.19811804T>G , CM000670.1:g.19811804T>G GRCh37
NC_000008.9:g.19856084T>G NCBI36
NG_008855.1:g.20223T>G
NG_008855.2:g.57577T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.715T>G MANE Select ENSP00000497642.1:p.Phe239Val
ENST00000311322.8:c.715T>G ENSP00000309757.6:p.Phe239Val
NM_000237.2:c.715T>G NP_000228.1:p.Phe239Val
NM_000237.3:c.715T>G MANE Select NP_000228.1:p.Phe239Val
Search 100 bp 5'
Search 100 bp 3'