Canonical Allele Identifier: CA674318972
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs1435144126
gnomAD v3: 11-1852790-G-A
gnomAD v4: 11-1852790-G-A
MyVariant Identifiers: chr11:g.1874020G>A (hg19) chr11:g.1852790G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852790G>A , CM000673.2:g.1852790G>A GRCh38
NC_000011.9:g.1874020G>A , CM000673.1:g.1874020G>A GRCh37
NC_000011.8:g.1830596G>A NCBI36
NG_011509.1:g.4821G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-163G>A ENSP00000502383.1:n.-192-163G>A
Search 100 bp 5'
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