Canonical Allele Identifier: CA453015919
Gene: LPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160969646G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548614G>T , CM000668.2:g.160548614G>T GRCh38
NC_000006.11:g.160969646G>T , CM000668.1:g.160969646G>T GRCh37
NC_000006.10:g.160889636G>T NCBI36
NG_016147.1:g.122762C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5019C>A MANE Select ENSP00000321334.6:p.Gly1673=
ENST00000316300.9:c.5019C>A ENSP00000321334.5:p.Gly1673=
NM_005577.2:c.5019C>A NP_005568.2:p.Gly1673=
NM_005577.3:c.5019C>A NP_005568.2:p.Gly1673=
NM_005577.4:c.5019C>A MANE Select NP_005568.2:p.Gly1673=
Search 100 bp 5'
Search 100 bp 3'