ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA589962183
Gene: LINC01492
HGNC
NCBI
Linked Data
dbSNP Id:
rs1283793187
gnomAD v2:
9-106024051-C-T
gnomAD v3:
9-103261769-C-T
gnomAD v4:
9-103261769-C-T
MyVariant Identifiers:
chr9:g.106024051C>T (hg19)
chr9:g.103261769C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103261769C>T , CM000671.2:g.103261769C>T
GRCh38
NC_000009.11:g.106024051C>T , CM000671.1:g.106024051C>T
GRCh37
NC_000009.10:g.105063872C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2755G>A
Search 100 bp 5'
Search 100 bp 3'