Canonical Allele Identifier: CA151230121
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs955166015
gnomAD v3: 6-160553573-T-A
gnomAD v4: 6-160553573-T-A
MyVariant Identifiers: chr6:g.160974605T>A (hg19) chr6:g.160553573T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553573T>A , CM000668.2:g.160553573T>A GRCh38
NC_000006.11:g.160974605T>A , CM000668.1:g.160974605T>A GRCh37
NC_000006.10:g.160894595T>A NCBI36
NG_016147.1:g.117803A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2452A>T MANE Select ENSP00000321334.6:n.4973+2452A>T
ENST00000316300.9:c.4973+2452A>T ENSP00000321334.5:n.4973+2452A>T
NM_005577.2:c.4973+2452A>T NP_005568.2:n.4973+2452A>T
NM_005577.3:c.4973+2452A>T NP_005568.2:n.4973+2452A>T
NM_005577.4:c.4973+2452A>T MANE Select NP_005568.2:n.4973+2452A>T
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