Canonical Allele Identifier: CA366352269
Gene: LPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160969639A>T (hg19) chr6:g.160548607A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548607A>T , CM000668.2:g.160548607A>T GRCh38
NC_000006.11:g.160969639A>T , CM000668.1:g.160969639A>T GRCh37
NC_000006.10:g.160889629A>T NCBI36
NG_016147.1:g.122769T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5026T>A MANE Select ENSP00000321334.6:p.Cys1676Ser
ENST00000316300.9:c.5026T>A ENSP00000321334.5:p.Cys1676Ser
NM_005577.2:c.5026T>A NP_005568.2:p.Cys1676Ser
NM_005577.3:c.5026T>A NP_005568.2:p.Cys1676Ser
NM_005577.4:c.5026T>A MANE Select NP_005568.2:p.Cys1676Ser
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