Canonical Allele Identifier: CA1947877280
Gene: LSP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852761G= , CM000673.2:g.1852761G= GRCh38
NC_000011.9:g.1873991G= , CM000673.1:g.1873991G= GRCh37
NC_000011.8:g.1830567G= NCBI36
NG_011509.1:g.4792G=

Transcript Alleles

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