Canonical Allele Identifier: CA1677116269
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1583574150
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553616C>A , CM000668.2:g.160553616C>A GRCh38
NC_000006.11:g.160974648C>A , CM000668.1:g.160974648C>A GRCh37
NC_000006.10:g.160894638C>A NCBI36
NG_016147.1:g.117760G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2409G>T MANE Select ENSP00000321334.6:n.4973+2409G>T
ENST00000316300.9:c.4973+2409G>T ENSP00000321334.5:n.4973+2409G>T
NM_005577.2:c.4973+2409G>T NP_005568.2:n.4973+2409G>T
NM_005577.3:c.4973+2409G>T NP_005568.2:n.4973+2409G>T
NM_005577.4:c.4973+2409G>T MANE Select NP_005568.2:n.4973+2409G>T
Search 100 bp 5'
Search 100 bp 3'