Canonical Allele Identifier: CA239777150
Gene: LINC02882 HGNC NCBI
dbSNP:
10506701
gnomAD v2:
12:74586210 T / G
gnomAD v3:
12:74192430 T / G
gnomAD v4:
chr12-74192430-T-G
Joint Max Group AF 0.19909986 (NFE)
Genomes Max Group AF 0.19909986 (NFE)
MyVariant.info:
GRCh38 chr12:g.74192430T>G
GRCh37 chr12:g.74586210T>G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.74192430T>G , CM000674.2:g.74192430T>G GRCh38
NC_000012.11:g.74586210T>G , CM000674.1:g.74586210T>G GRCh37
NC_000012.10:g.72872477T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038300.1:n.553+1644A>C
Search 100 bp 5'
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