Canonical Allele Identifier: CA1947877296
Gene: LSP1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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