Canonical Allele Identifier: CA2611933831
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852882-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852882C>T , CM000673.2:g.1852882C>T GRCh38
NC_000011.9:g.1874112C>T , CM000673.1:g.1874112C>T GRCh37
NC_000011.8:g.1830688C>T NCBI36
NG_011509.1:g.4913C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676039.1:c.-192-71C>T ENSP00000502383.1:n.-192-71C>T
Search 100 bp 5'
Search 100 bp 3'