Canonical Allele Identifier: CA2611933805
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852872-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852872C>A , CM000673.2:g.1852872C>A GRCh38
NC_000011.9:g.1874102C>A , CM000673.1:g.1874102C>A GRCh37
NC_000011.8:g.1830678C>A NCBI36
NG_011509.1:g.4903C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000676039.1:c.-192-81C>A ENSP00000502383.1:n.-192-81C>A