Canonical Allele Identifier: CA366352298
Gene: LPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160969645G>C (hg19) chr6:g.160548613G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548613G>C , CM000668.2:g.160548613G>C GRCh38
NC_000006.11:g.160969645G>C , CM000668.1:g.160969645G>C GRCh37
NC_000006.10:g.160889635G>C NCBI36
NG_016147.1:g.122763C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5020C>G MANE Select ENSP00000321334.6:p.Pro1674Ala
ENST00000316300.9:c.5020C>G ENSP00000321334.5:p.Pro1674Ala
NM_005577.2:c.5020C>G NP_005568.2:p.Pro1674Ala
NM_005577.3:c.5020C>G NP_005568.2:p.Pro1674Ala
NM_005577.4:c.5020C>G MANE Select NP_005568.2:p.Pro1674Ala
Search 100 bp 5'
Search 100 bp 3'