Canonical Allele Identifier: CA1947877422
Gene: LSP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852873A= , CM000673.2:g.1852873A= GRCh38
NC_000011.9:g.1874103A= , CM000673.1:g.1874103A= GRCh37
NC_000011.8:g.1830679A= NCBI36
NG_011509.1:g.4904A=

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-80A= ENSP00000502383.1:n.-192-80A=