Canonical Allele Identifier: CA962595899
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs1948766016
gnomAD v3: 14-44637496-T-C
gnomAD v4: 14-44637496-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637496T>C , CM000676.2:g.44637496T>C GRCh38
NC_000014.8:g.45106699T>C , CM000676.1:g.45106699T>C GRCh37
NC_000014.7:g.44176449T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40483A>G
XR_943801.1:n.226-40483A>G
XR_943806.1:n.226-40483A>G
XR_943808.1:n.126+160434A>G
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