Canonical Allele Identifier: CA1096555557
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1778198268
gnomAD v3: 6-160553475-T-C
gnomAD v4: 6-160553475-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553475T>C , CM000668.2:g.160553475T>C GRCh38
NC_000006.11:g.160974507T>C , CM000668.1:g.160974507T>C GRCh37
NC_000006.10:g.160894497T>C NCBI36
NG_016147.1:g.117901A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2550A>G MANE Select ENSP00000321334.6:n.4973+2550A>G
ENST00000316300.9:c.4973+2550A>G ENSP00000321334.5:n.4973+2550A>G
NM_005577.2:c.4973+2550A>G NP_005568.2:n.4973+2550A>G
NM_005577.3:c.4973+2550A>G NP_005568.2:n.4973+2550A>G
NM_005577.4:c.4973+2550A>G MANE Select NP_005568.2:n.4973+2550A>G
Search 100 bp 5'
Search 100 bp 3'