Canonical Allele Identifier: CA821619713
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1265003685
gnomAD v3: 6-160553610-C-T
gnomAD v4: 6-160553610-C-T
MyVariant Identifiers: chr6:g.160974642C>T (hg19) chr6:g.160553610C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553610C>T , CM000668.2:g.160553610C>T GRCh38
NC_000006.11:g.160974642C>T , CM000668.1:g.160974642C>T GRCh37
NC_000006.10:g.160894632C>T NCBI36
NG_016147.1:g.117766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2415G>A MANE Select ENSP00000321334.6:n.4973+2415G>A
ENST00000316300.9:c.4973+2415G>A ENSP00000321334.5:n.4973+2415G>A
NM_005577.2:c.4973+2415G>A NP_005568.2:n.4973+2415G>A
NM_005577.3:c.4973+2415G>A NP_005568.2:n.4973+2415G>A
NM_005577.4:c.4973+2415G>A MANE Select NP_005568.2:n.4973+2415G>A
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