Canonical Allele Identifier: CA2681082795
Gene: LPA HGNC NCBI

Linked Data

gnomAD v4: 6-160548710-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548710G>A , CM000668.2:g.160548710G>A GRCh38
NC_000006.11:g.160969742G>A , CM000668.1:g.160969742G>A GRCh37
NC_000006.10:g.160889732G>A NCBI36
NG_016147.1:g.122666C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-51C>T MANE Select ENSP00000321334.6:n.4974-51C>T
ENST00000316300.9:c.4974-51C>T ENSP00000321334.5:n.4974-51C>T
NM_005577.2:c.4974-51C>T NP_005568.2:n.4974-51C>T
NM_005577.3:c.4974-51C>T NP_005568.2:n.4974-51C>T
NM_005577.4:c.4974-51C>T MANE Select NP_005568.2:n.4974-51C>T
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