Canonical Allele Identifier: CA597057520
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs1166954935
gnomAD v2: 11-1873880-G-A
MyVariant Identifiers: chr11:g.1873880G>A (hg19) chr11:g.1852650G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852650G>A , CM000673.2:g.1852650G>A GRCh38
NC_000011.9:g.1873880G>A , CM000673.1:g.1873880G>A GRCh37
NC_000011.8:g.1830456G>A NCBI36
NG_011509.1:g.4681G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000676039.1:c.-192-303G>A ENSP00000502383.1:n.-192-303G>A
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