ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA466833021
Gene: LINC02977
HGNC
NCBI
Linked Data
dbSNP Id:
rs10125054
MyVariant Identifiers:
chr9:g.114798037G>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.112035757G>C , CM000671.2:g.112035757G>C
GRCh38
NC_000009.11:g.114798037G>C , CM000671.1:g.114798037G>C
GRCh37
NC_000009.10:g.113837858G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_930251.3:n.2186+2422C>G
Search 100 bp 5'
Search 100 bp 3'