Canonical Allele Identifier: CA571544608

Gene: LPA

Linked Data

• dbSNP Id: rs1477664467
• gnomAD v2: 6-160974591-A-G
• gnomAD v3: 6-160553559-A-G
• gnomAD v4: 6-160553559-A-G
• MyVariant Identifiers: chr6:g.160974591A>G (hg19) ; chr6:g.160553559A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553559A>G , CM000668.2:g.160553559A>G	GRCh38
NC_000006.11:g.160974591A>G , CM000668.1:g.160974591A>G	GRCh37
NC_000006.10:g.160894581A>G	NCBI36
NG_016147.1:g.117817T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.4973+2466T>C MANE Select	ENSP00000321334.6:n.4973+2466T>C
ENST00000316300.9:c.4973+2466T>C	ENSP00000321334.5:n.4973+2466T>C
NM_005577.2:c.4973+2466T>C	NP_005568.2:n.4973+2466T>C
NM_005577.3:c.4973+2466T>C	NP_005568.2:n.4973+2466T>C
NM_005577.4:c.4973+2466T>C MANE Select	NP_005568.2:n.4973+2466T>C