ClinGen Allele Registry
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Canonical Allele Identifier:
CA85231859
Gene: LINC02045
HGNC
NCBI
Linked Data
dbSNP Id:
rs1456669
gnomAD v2:
3-147935635-C-A
gnomAD v3:
3-148217848-C-A
gnomAD v4:
3-148217848-C-A
MyVariant Identifiers:
chr3:g.147935635C>A (hg19)
chr3:g.148217848C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148217848C>A , CM000665.2:g.148217848C>A
GRCh38
NC_000003.11:g.147935635C>A , CM000665.1:g.147935635C>A
GRCh37
NC_000003.10:g.149418325C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_924565.1:n.86+2662G>T
Search 100 bp 5'
Search 100 bp 3'