Canonical Allele Identifier: CA13200987
Gene: LINC01475 HGNC NCBI
dbSNP:
10883365
gnomAD v2:
10:101287764 G / A
gnomAD v3:
10:99528007 G / A
gnomAD v4:
chr10-99528007-G-A
Joint Max Group AF 0.60779069 (SAS)
Genomes Max Group AF 0.60804205 (SAS)
Exomes Max Group AF 0.3868618 (AFR)
MyVariant.info:
GRCh38 chr10:g.99528007G>A
GRCh37 chr10:g.101287764G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528007G>A , CM000672.2:g.99528007G>A GRCh38
NC_000010.10:g.101287764G>A , CM000672.1:g.101287764G>A GRCh37
NC_000010.9:g.101277754G>A NCBI36
NG_016854.1:g.75G>A

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.376C>T
Search 100 bp 5'
Search 100 bp 3'