Canonical Allele Identifier: CA239777150
Gene: LINC02882 HGNC NCBI

Linked Data

dbSNP Id: rs10506701
gnomAD v2: 12-74586210-T-G
gnomAD v3: 12-74192430-T-G
gnomAD v4: 12-74192430-T-G
MyVariant Identifiers: chr12:g.74586210T>G (hg19) chr12:g.74192430T>G (hg38)
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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
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