Canonical Allele Identifier: CA216187390
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs534064618
gnomAD v3: 11-1852784-T-C
gnomAD v4: 11-1852784-T-C
MyVariant Identifiers: chr11:g.1874014T>C (hg19) chr11:g.1852784T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852784T>C , CM000673.2:g.1852784T>C GRCh38
NC_000011.9:g.1874014T>C , CM000673.1:g.1874014T>C GRCh37
NC_000011.8:g.1830590T>C NCBI36
NG_011509.1:g.4815T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-169T>C ENSP00000502383.1:n.-192-169T>C
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