Canonical Allele Identifier: CA459879421
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590143226
MyVariant Identifiers: chr8:g.19811698A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954187A>T , CM000670.2:g.19954187A>T GRCh38
NC_000008.10:g.19811698A>T , CM000670.1:g.19811698A>T GRCh37
NC_000008.9:g.19855978A>T NCBI36
NG_008855.1:g.20117A>T
NG_008855.2:g.57471A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.609A>T MANE Select ENSP00000497642.1:p.Ala203=
ENST00000311322.8:c.609A>T ENSP00000309757.6:p.Ala203=
NM_000237.2:c.609A>T NP_000228.1:p.Ala203=
NM_000237.3:c.609A>T MANE Select NP_000228.1:p.Ala203=