Canonical Allele Identifier: CA571544613

Gene: LPA

Linked Data

• dbSNP Id: rs1400340281
• gnomAD v2: 6-160974678-T-C
• gnomAD v3: 6-160553646-T-C
• gnomAD v4: 6-160553646-T-C
• MyVariant Identifiers: chr6:g.160974678T>C (hg19) ; chr6:g.160553646T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553646T>C , CM000668.2:g.160553646T>C	GRCh38
NC_000006.11:g.160974678T>C , CM000668.1:g.160974678T>C	GRCh37
NC_000006.10:g.160894668T>C	NCBI36
NG_016147.1:g.117730A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4973+2379A>G MANE Select	ENSP00000321334.6:n.4973+2379A>G
ENST00000316300.9:c.4973+2379A>G	ENSP00000321334.5:n.4973+2379A>G
NM_005577.2:c.4973+2379A>G	NP_005568.2:n.4973+2379A>G
NM_005577.3:c.4973+2379A>G	NP_005568.2:n.4973+2379A>G
NM_005577.4:c.4973+2379A>G MANE Select	NP_005568.2:n.4973+2379A>G