Canonical Allele Identifier: CA10948888
Gene: LINC02774 HGNC NCBI

Linked Data

dbSNP Id: rs12127679
gnomAD v2: 1-244167801-C-T
gnomAD v3: 1-244004499-C-T
gnomAD v4: 1-244004499-C-T
MyVariant Identifiers: chr1:g.244167801C>T (hg19) chr1:g.244004499C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244004499C>T , CM000663.2:g.244004499C>T GRCh38
NC_000001.10:g.244167801C>T , CM000663.1:g.244167801C>T GRCh37
NC_000001.9:g.242234424C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033883.1:n.354-559C>T
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