Canonical Allele Identifier: CA216187417
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs939071284
MyVariant Identifiers: chr11:g.1874023C>A (hg19) chr11:g.1852793C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852793C>A , CM000673.2:g.1852793C>A GRCh38
NC_000011.9:g.1874023C>A , CM000673.1:g.1874023C>A GRCh37
NC_000011.8:g.1830599C>A NCBI36
NG_011509.1:g.4824C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-160C>A ENSP00000502383.1:n.-192-160C>A
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