Canonical Allele Identifier: CA1769104319
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069978071
gnomAD v4: 8-19955693-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955693A>T , CM000670.2:g.19955693A>T GRCh38
NC_000008.10:g.19813204A>T , CM000670.1:g.19813204A>T GRCh37
NC_000008.9:g.19857484A>T NCBI36
NG_008855.1:g.21623A>T
NG_008855.2:g.58977A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-148A>T MANE Select ENSP00000497642.1:n.776-148A>T
ENST00000311322.8:c.776-148A>T ENSP00000309757.6:n.776-148A>T
NM_000237.2:c.776-148A>T NP_000228.1:n.776-148A>T
NM_000237.3:c.776-148A>T MANE Select NP_000228.1:n.776-148A>T