Canonical Allele Identifier: CA366352306
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1249853765
gnomAD v2: 6-160969647-C-T
gnomAD v4: 6-160548615-C-T
MyVariant Identifiers: chr6:g.160969647C>T (hg19) chr6:g.160548615C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548615C>T , CM000668.2:g.160548615C>T GRCh38
NC_000006.11:g.160969647C>T , CM000668.1:g.160969647C>T GRCh37
NC_000006.10:g.160889637C>T NCBI36
NG_016147.1:g.122761G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5018G>A MANE Select ENSP00000321334.6:p.Gly1673Asp
ENST00000316300.9:c.5018G>A ENSP00000321334.5:p.Gly1673Asp
NM_005577.2:c.5018G>A NP_005568.2:p.Gly1673Asp
NM_005577.3:c.5018G>A NP_005568.2:p.Gly1673Asp
NM_005577.4:c.5018G>A MANE Select NP_005568.2:p.Gly1673Asp
Search 100 bp 5'
Search 100 bp 3'