Canonical Allele Identifier: CA370468669
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954315-G-T
MyVariant Identifiers: chr8:g.19811826G>T (hg19) chr8:g.19954315G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954315G>T , CM000670.2:g.19954315G>T GRCh38
NC_000008.10:g.19811826G>T , CM000670.1:g.19811826G>T GRCh37
NC_000008.9:g.19856106G>T NCBI36
NG_008855.1:g.20245G>T
NG_008855.2:g.57599G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.737G>T MANE Select ENSP00000497642.1:p.Gly246Val
ENST00000311322.8:c.737G>T ENSP00000309757.6:p.Gly246Val
NM_000237.2:c.737G>T NP_000228.1:p.Gly246Val
NM_000237.3:c.737G>T MANE Select NP_000228.1:p.Gly246Val
Search 100 bp 5'
Search 100 bp 3'