Canonical Allele Identifier: CA10768355
Gene: LINC02786 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.38136401C>A
GRCh37 chr1:g.38602073C>A
gnomAD v2:
1:38602073 C / A
gnomAD v3:
1:38136401 C / A
gnomAD v4:
chr1-38136401-C-A
Joint Max Group AF 0.16982015 (EAS)
Genomes Max Group AF 0.16982015 (EAS)
Exomes Max Group AF 0.01110501 (NFE)
dbSNP:
7547921
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38136401C>A , CM000663.2:g.38136401C>A GRCh38
NC_000001.10:g.38602073C>A , CM000663.1:g.38602073C>A GRCh37
NC_000001.9:g.38374660C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947206.1:n.227G>T
XR_947207.1:n.99G>T
XR_947208.1:n.227G>T
XR_001737989.2:n.1236G>T
XR_001737990.2:n.2251G>T
XR_001737991.2:n.99G>T
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