Canonical Allele Identifier: CA15987949
Gene: LINC02940 HGNC NCBI
MyVariant.info:
GRCh38 chr21:g.39008323C>T
GRCh37 chr21:g.40380249C>T
gnomAD v2:
21:40380249 C / T
gnomAD v3:
21:39008323 C / T
gnomAD v4:
chr21-39008323-C-T
Joint Max Group AF 0.44497566 (NFE)
Genomes Max Group AF 0.44492965 (NFE)
Exomes Max Group AF 0.34952591 (NFE)
dbSNP:
2836823
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.39008323C>T , CM000683.2:g.39008323C>T GRCh38
NC_000021.8:g.40380249C>T , CM000683.1:g.40380249C>T GRCh37
NC_000021.7:g.39302119C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_430375.2:n.1392-1539G>A
XR_937714.1:n.1375-1539G>A
XR_937715.1:n.1240-1539G>A
XR_937716.1:n.1219-1539G>A
XR_001755043.2:n.2115-1539G>A
XR_001755044.2:n.1341-1539G>A
XR_001755045.2:n.1392-1539G>A
XR_001755046.2:n.1392-1539G>A
XR_001755047.2:n.1392-1539G>A
XR_001755048.2:n.609-1539G>A
XR_001755049.2:n.1392-1539G>A
XR_430375.4:n.1392-1539G>A
XR_937714.3:n.1375-1539G>A
XR_937715.3:n.1240-1539G>A
XR_937716.3:n.1221-1539G>A
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