Canonical Allele Identifier: CA14047725
Gene: LINC02302 HGNC NCBI

Linked Data

dbSNP Id: rs12884395
gnomAD v2: 14-45106632-A-G
gnomAD v3: 14-44637429-A-G
gnomAD v4: 14-44637429-A-G
MyVariant Identifiers: chr14:g.45106632A>G (hg19) chr14:g.44637429A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.44637429A>G , CM000676.2:g.44637429A>G GRCh38
NC_000014.8:g.45106632A>G , CM000676.1:g.45106632A>G GRCh37
NC_000014.7:g.44176382A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943800.1:n.226-40416T>C
XR_943801.1:n.226-40416T>C
XR_943806.1:n.226-40416T>C
XR_943808.1:n.126+160501T>C
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