Canonical Allele Identifier: CA13694792
Gene: LINC02456 HGNC NCBI
gnomAD v2:
12:102787814 A / G
gnomAD v3:
12:102394036 A / G
gnomAD v4:
chr12-102394036-A-G
Joint Max Group AF 0.67704875 (NFE)
Genomes Max Group AF 0.67704211 (NFE)
Exomes Max Group AF 0.3875281 (NFE)
dbSNP:
2946834
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102394036A>G , CM000674.2:g.102394036A>G GRCh38
NC_000012.11:g.102787814A>G , CM000674.1:g.102787814A>G GRCh37
NC_000012.10:g.101311944A>G NCBI36
NG_011713.1:g.91565T>C

Transcript Alleles

HGVS Amino-acid Change
XR_945270.1:n.582-10077A>G
XR_945271.1:n.582-10077A>G
XR_945272.1:n.582-10077A>G
XR_945273.1:n.532-10077A>G
XR_945274.1:n.258-10077A>G
XR_945275.1:n.138-10077A>G
XR_945276.1:n.110-10077A>G
XR_945277.1:n.582-10077A>G
XR_001749285.1:n.697-10077A>G
XR_001749286.1:n.258-10077A>G
XR_001749287.1:n.576-10077A>G
XR_001749288.1:n.1585-10077A>G
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