Canonical Allele Identifier: CA151230165

Gene: LPA

Linked Data

• dbSNP Id: rs568670520
• gnomAD v3: 6-160553603-T-G
• gnomAD v4: 6-160553603-T-G
• MyVariant Identifiers: chr6:g.160974635T>G (hg19) ; chr6:g.160553603T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553603T>G , CM000668.2:g.160553603T>G	GRCh38
NC_000006.11:g.160974635T>G , CM000668.1:g.160974635T>G	GRCh37
NC_000006.10:g.160894625T>G	NCBI36
NG_016147.1:g.117773A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4973+2422A>C MANE Select	ENSP00000321334.6:n.4973+2422A>C
ENST00000316300.9:c.4973+2422A>C	ENSP00000321334.5:n.4973+2422A>C
NM_005577.2:c.4973+2422A>C	NP_005568.2:n.4973+2422A>C
NM_005577.3:c.4973+2422A>C	NP_005568.2:n.4973+2422A>C
NM_005577.4:c.4973+2422A>C MANE Select	NP_005568.2:n.4973+2422A>C