Canonical Allele Identifier: CA366352281
Gene: LPA HGNC NCBI

Linked Data

gnomAD v4: 6-160548609-C-T
MyVariant Identifiers: chr6:g.160969641C>T (hg19) chr6:g.160548609C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548609C>T , CM000668.2:g.160548609C>T GRCh38
NC_000006.11:g.160969641C>T , CM000668.1:g.160969641C>T GRCh37
NC_000006.10:g.160889631C>T NCBI36
NG_016147.1:g.122767G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5024G>A MANE Select ENSP00000321334.6:p.Trp1675Ter
ENST00000316300.9:c.5024G>A ENSP00000321334.5:p.Trp1675Ter
NM_005577.2:c.5024G>A NP_005568.2:p.Trp1675Ter
NM_005577.3:c.5024G>A NP_005568.2:p.Trp1675Ter
NM_005577.4:c.5024G>A MANE Select NP_005568.2:p.Trp1675Ter
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