Canonical Allele Identifier: CA1677112015
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1778121733
gnomAD v4: 6-160548725-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548725C>T , CM000668.2:g.160548725C>T GRCh38
NC_000006.11:g.160969757C>T , CM000668.1:g.160969757C>T GRCh37
NC_000006.10:g.160889747C>T NCBI36
NG_016147.1:g.122651G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-66G>A MANE Select ENSP00000321334.6:n.4974-66G>A
ENST00000316300.9:c.4974-66G>A ENSP00000321334.5:n.4974-66G>A
NM_005577.2:c.4974-66G>A NP_005568.2:n.4974-66G>A
NM_005577.3:c.4974-66G>A NP_005568.2:n.4974-66G>A
NM_005577.4:c.4974-66G>A MANE Select NP_005568.2:n.4974-66G>A
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