Canonical Allele Identifier: CA370469042
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19955894-G-T
MyVariant Identifiers: chr8:g.19813405G>T (hg19) chr8:g.19955894G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955894G>T , CM000670.2:g.19955894G>T GRCh38
NC_000008.10:g.19813405G>T , CM000670.1:g.19813405G>T GRCh37
NC_000008.9:g.19857685G>T NCBI36
NG_008855.1:g.21824G>T
NG_008855.2:g.59178G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.829G>T MANE Select ENSP00000497642.1:p.Asp277Tyr
ENST00000311322.8:c.829G>T ENSP00000309757.6:p.Asp277Tyr
NM_000237.2:c.829G>T NP_000228.1:p.Asp277Tyr
NM_000237.3:c.829G>T MANE Select NP_000228.1:p.Asp277Tyr
Search 100 bp 5'
Search 100 bp 3'