Canonical Allele Identifier: CA264594501
Gene: LINC02301 HGNC NCBI

Linked Data

dbSNP Id: rs1242541
gnomAD v2: 14-83206037-A-G
gnomAD v3: 14-82739693-A-G
gnomAD v4: 14-82739693-A-G
MyVariant Identifiers: chr14:g.83206037A>G (hg19) chr14:g.82739693A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.82739693A>G , CM000676.2:g.82739693A>G GRCh38
NC_000014.8:g.83206037A>G , CM000676.1:g.83206037A>G GRCh37
NC_000014.7:g.82275790A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944088.1:n.362-1006A>G
Search 100 bp 5'
Search 100 bp 3'