Canonical Allele Identifier: CA613969002
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1425608325
gnomAD v2: 14-45106567-G-A
gnomAD v3: 14-44637364-G-A
gnomAD v4: 14-44637364-G-A
MyVariant Identifiers: chr14:g.45106567G>A (hg19) chr14:g.44637364G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637364G>A , CM000676.2:g.44637364G>A GRCh38
NC_000014.8:g.45106567G>A , CM000676.1:g.45106567G>A GRCh37
NC_000014.7:g.44176317G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40351C>T
XR_943801.1:n.226-40351C>T
XR_943806.1:n.226-40351C>T
XR_943808.1:n.126+160566C>T
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