Canonical Allele Identifier: CA370468448
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811724T>C (hg19) chr8:g.19954213T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954213T>C , CM000670.2:g.19954213T>C GRCh38
NC_000008.10:g.19811724T>C , CM000670.1:g.19811724T>C GRCh37
NC_000008.9:g.19856004T>C NCBI36
NG_008855.1:g.20143T>C
NG_008855.2:g.57497T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.635T>C MANE Select ENSP00000497642.1:p.Phe212Ser
ENST00000311322.8:c.635T>C ENSP00000309757.6:p.Phe212Ser
NM_000237.2:c.635T>C NP_000228.1:p.Phe212Ser
NM_000237.3:c.635T>C MANE Select NP_000228.1:p.Phe212Ser
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