Canonical Allele Identifier: CA2611933755
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852845-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852845A>C , CM000673.2:g.1852845A>C GRCh38
NC_000011.9:g.1874075A>C , CM000673.1:g.1874075A>C GRCh37
NC_000011.8:g.1830651A>C NCBI36
NG_011509.1:g.4876A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-108A>C ENSP00000502383.1:n.-192-108A>C