Canonical Allele Identifier: CA706048957
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1325235556
gnomAD v3: 14-44637278-T-C
gnomAD v4: 14-44637278-T-C
MyVariant Identifiers: chr14:g.45106481T>C (hg19) chr14:g.44637278T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637278T>C , CM000676.2:g.44637278T>C GRCh38
NC_000014.8:g.45106481T>C , CM000676.1:g.45106481T>C GRCh37
NC_000014.7:g.44176231T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40265A>G
XR_943801.1:n.226-40265A>G
XR_943806.1:n.226-40265A>G
XR_943808.1:n.126+160652A>G
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