Canonical Allele Identifier: CA151230162
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs982622698
MyVariant Identifiers: chr6:g.160974622A>G (hg19) chr6:g.160553590A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553590A>G , CM000668.2:g.160553590A>G GRCh38
NC_000006.11:g.160974622A>G , CM000668.1:g.160974622A>G GRCh37
NC_000006.10:g.160894612A>G NCBI36
NG_016147.1:g.117786T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4973+2435T>C MANE Select ENSP00000321334.6:n.4973+2435T>C
ENST00000316300.9:c.4973+2435T>C ENSP00000321334.5:n.4973+2435T>C
NM_005577.2:c.4973+2435T>C NP_005568.2:n.4973+2435T>C
NM_005577.3:c.4973+2435T>C NP_005568.2:n.4973+2435T>C
NM_005577.4:c.4973+2435T>C MANE Select NP_005568.2:n.4973+2435T>C
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