Canonical Allele Identifier: CA453015928
Gene: LPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160969649T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548617T>A , CM000668.2:g.160548617T>A GRCh38
NC_000006.11:g.160969649T>A , CM000668.1:g.160969649T>A GRCh37
NC_000006.10:g.160889639T>A NCBI36
NG_016147.1:g.122759A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5016A>T MANE Select ENSP00000321334.6:p.Thr1672=
ENST00000316300.9:c.5016A>T ENSP00000321334.5:p.Thr1672=
NM_005577.2:c.5016A>T NP_005568.2:p.Thr1672=
NM_005577.3:c.5016A>T NP_005568.2:p.Thr1672=
NM_005577.4:c.5016A>T MANE Select NP_005568.2:p.Thr1672=
Search 100 bp 5'
Search 100 bp 3'