Canonical Allele Identifier: CA453015934
Gene: LPA HGNC NCBI

Linked Data

gnomAD v4: 6-160548617-T-G
MyVariant Identifiers: chr6:g.160969649T>G (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5016A>C MANE Select ENSP00000321334.6:p.Thr1672=
ENST00000316300.9:c.5016A>C ENSP00000321334.5:p.Thr1672=
NM_005577.2:c.5016A>C NP_005568.2:p.Thr1672=
NM_005577.3:c.5016A>C NP_005568.2:p.Thr1672=
NM_005577.4:c.5016A>C MANE Select NP_005568.2:p.Thr1672=
Search 100 bp 5'
Search 100 bp 3'