Canonical Allele Identifier: CA15665572
Gene: LINC02625 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.61781965G>T
GRCh37 chr10:g.63541723G>T
gnomAD v2:
10:63541723 G / T
gnomAD v3:
10:61781965 G / T
gnomAD v4:
chr10-61781965-G-T
Joint Max Group AF 0.20193827 (AMR)
Genomes Max Group AF 0.20193827 (AMR)
Exomes Max Group AF 0.11168225 (NFE)
dbSNP:
751891
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61781965G>T , CM000672.2:g.61781965G>T GRCh38
NC_000010.10:g.63541723G>T , CM000672.1:g.63541723G>T GRCh37
NC_000010.9:g.63211729G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747458.1:n.436-126C>A
XR_001747459.1:n.559-126C>A
XR_001747460.1:n.597-126C>A
XR_001747461.1:n.435+263C>A
XR_001747462.1:n.527-126C>A
XR_001747463.1:n.326-126C>A
XR_002957080.1:n.558+263C>A
XR_002957081.1:n.396+263C>A
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