Canonical Allele Identifier: CA571544611
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1406251842
gnomAD v2: 6-160974644-C-A
gnomAD v3: 6-160553612-C-A
gnomAD v4: 6-160553612-C-A
MyVariant Identifiers: chr6:g.160974644C>A (hg19) chr6:g.160553612C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553612C>A , CM000668.2:g.160553612C>A GRCh38
NC_000006.11:g.160974644C>A , CM000668.1:g.160974644C>A GRCh37
NC_000006.10:g.160894634C>A NCBI36
NG_016147.1:g.117764G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2413G>T MANE Select ENSP00000321334.6:n.4973+2413G>T
ENST00000316300.9:c.4973+2413G>T ENSP00000321334.5:n.4973+2413G>T
NM_005577.2:c.4973+2413G>T NP_005568.2:n.4973+2413G>T
NM_005577.3:c.4973+2413G>T NP_005568.2:n.4973+2413G>T
NM_005577.4:c.4973+2413G>T MANE Select NP_005568.2:n.4973+2413G>T
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