Canonical Allele Identifier: CA366352322
Gene: LPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160969652A>C (hg19) chr6:g.160548620A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548620A>C , CM000668.2:g.160548620A>C GRCh38
NC_000006.11:g.160969652A>C , CM000668.1:g.160969652A>C GRCh37
NC_000006.10:g.160889642A>C NCBI36
NG_016147.1:g.122756T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5013T>G MANE Select ENSP00000321334.6:p.Asp1671Glu
ENST00000316300.9:c.5013T>G ENSP00000321334.5:p.Asp1671Glu
NM_005577.2:c.5013T>G NP_005568.2:p.Asp1671Glu
NM_005577.3:c.5013T>G NP_005568.2:p.Asp1671Glu
NM_005577.4:c.5013T>G MANE Select NP_005568.2:p.Asp1671Glu
Search 100 bp 5'
Search 100 bp 3'