ClinGen Allele Registry
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Canonical Allele Identifier:
CA1054734259
Gene: LINC02045
HGNC
NCBI
Linked Data
dbSNP Id:
rs1041835687
gnomAD v3:
3-148217611-C-A
gnomAD v4:
3-148217611-C-A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148217611C>A , CM000665.2:g.148217611C>A
GRCh38
NC_000003.11:g.147935398C>A , CM000665.1:g.147935398C>A
GRCh37
NC_000003.10:g.149418088C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_924565.1:n.86+2899G>T
Search 100 bp 5'
Search 100 bp 3'