Canonical Allele Identifier: CA260254660
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs757776727
gnomAD v3: 14-44637346-CA-C
gnomAD v4: 14-44637346-CA-C
MyVariant Identifiers: chr14:g.45106550del (hg19) chr14:g.44637347del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637348del , CM000676.2:g.44637348del GRCh38
NC_000014.8:g.45106551del , CM000676.1:g.45106551del GRCh37
NC_000014.7:g.44176301del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943800.1:n.226-40334del
XR_943801.1:n.226-40334del
XR_943806.1:n.226-40334del
XR_943808.1:n.126+160583del
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