Canonical Allele Identifier: CA4085890
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs776953380
ExAC: 6:160969743 A / C
gnomAD v2: 6-160969743-A-C
gnomAD v4: 6-160548711-A-C
MyVariant Identifiers: chr6:g.160969743A>C (hg19) chr6:g.160548711A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548711A>C , CM000668.2:g.160548711A>C GRCh38
NC_000006.11:g.160969743A>C , CM000668.1:g.160969743A>C GRCh37
NC_000006.10:g.160889733A>C NCBI36
NG_016147.1:g.122665T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-52T>G MANE Select ENSP00000321334.6:n.4974-52T>G
ENST00000316300.9:c.4974-52T>G ENSP00000321334.5:n.4974-52T>G
NM_005577.2:c.4974-52T>G NP_005568.2:n.4974-52T>G
NM_005577.3:c.4974-52T>G NP_005568.2:n.4974-52T>G
NM_005577.4:c.4974-52T>G MANE Select NP_005568.2:n.4974-52T>G
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