Canonical Allele Identifier: CA13405990
Gene: LSP1 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.1852842G>A
GRCh37 chr11:g.1874072G>A
gnomAD v2:
11:1874072 G / A
gnomAD v3:
11:1852842 G / A
gnomAD v4:
chr11-1852842-G-A
Joint Max Group AF 0.33598294 (AMR)
Genomes Max Group AF 0.32329739 (AMR)
Exomes Max Group AF 0.34602863 (AMR)
dbSNP:
907611
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852842G>A , CM000673.2:g.1852842G>A GRCh38
NC_000011.9:g.1874072G>A , CM000673.1:g.1874072G>A GRCh37
NC_000011.8:g.1830648G>A NCBI36
NG_011509.1:g.4873G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000676039.1:c.-192-111G>A ENSP00000502383.1:n.-192-111G>A
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