Canonical Allele Identifier: CA2611933802
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852870-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852870G>T , CM000673.2:g.1852870G>T GRCh38
NC_000011.9:g.1874100G>T , CM000673.1:g.1874100G>T GRCh37
NC_000011.8:g.1830676G>T NCBI36
NG_011509.1:g.4901G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676039.1:c.-192-83G>T ENSP00000502383.1:n.-192-83G>T