ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA85231829
Gene: LINC02045
HGNC
NCBI
Linked Data
dbSNP Id:
rs1016755133
gnomAD v3:
3-148217753-T-C
gnomAD v4:
3-148217753-T-C
MyVariant Identifiers:
chr3:g.147935540T>C (hg19)
chr3:g.148217753T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148217753T>C , CM000665.2:g.148217753T>C
GRCh38
NC_000003.11:g.147935540T>C , CM000665.1:g.147935540T>C
GRCh37
NC_000003.10:g.149418230T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_924565.1:n.86+2757A>G
Search 100 bp 5'
Search 100 bp 3'