Canonical Allele Identifier: CA2611933772
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852855-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852855T>A , CM000673.2:g.1852855T>A GRCh38
NC_000011.9:g.1874085T>A , CM000673.1:g.1874085T>A GRCh37
NC_000011.8:g.1830661T>A NCBI36
NG_011509.1:g.4886T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-98T>A ENSP00000502383.1:n.-192-98T>A