Canonical Allele Identifier: CA43055513
Gene: LINC00276 HGNC NCBI

Linked Data

dbSNP Id: rs16861531
gnomAD v2: 2-14398052-G-C
gnomAD v3: 2-14257928-G-C
gnomAD v4: 2-14257928-G-C
MyVariant Identifiers: chr2:g.14398052G>C (hg19) chr2:g.14257928G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.14257928G>C , CM000664.2:g.14257928G>C GRCh38
NC_000002.11:g.14398052G>C , CM000664.1:g.14398052G>C GRCh37
NC_000002.10:g.14315503G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103814.2:n.252-21978C>G
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