Canonical Allele Identifier: CA11145016
Gene: LINC00299 HGNC NCBI
dbSNP:
10174949
gnomAD v2:
2:8442248 G / A
gnomAD v3:
2:8302118 G / A
gnomAD v4:
chr2-8302118-G-A
Joint Max Group AF 0.27939759 (NFE)
Genomes Max Group AF 0.27939759 (NFE)
MyVariant.info:
GRCh38 chr2:g.8302118G>A
GRCh37 chr2:g.8442248G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.8302118G>A , CM000664.2:g.8302118G>A GRCh38
NC_000002.11:g.8442248G>A , CM000664.1:g.8442248G>A GRCh37
NC_000002.10:g.8359699G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034135.1:n.330-2325C>T
NR_152741.1:n.454-2325C>T
Search 100 bp 5'
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