Canonical Allele Identifier: CA571543802
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1353744305
gnomAD v2: 6-160962513-C-T
gnomAD v3: 6-160541481-C-T
gnomAD v4: 6-160541481-C-T
MyVariant Identifiers: chr6:g.160962513C>T (hg19) chr6:g.160541481C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541481C>T , CM000668.2:g.160541481C>T GRCh38
NC_000006.11:g.160962513C>T , CM000668.1:g.160962513C>T GRCh37
NC_000006.10:g.160882503C>T NCBI36
NG_016147.1:g.129895G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-300G>A MANE Select ENSP00000321334.6:n.5520-300G>A
ENST00000316300.9:c.5520-300G>A ENSP00000321334.5:n.5520-300G>A
NM_005577.2:c.5520-300G>A NP_005568.2:n.5520-300G>A
NM_005577.3:c.5520-300G>A NP_005568.2:n.5520-300G>A
NM_005577.4:c.5520-300G>A MANE Select NP_005568.2:n.5520-300G>A
Search 100 bp 5'
Search 100 bp 3'