ClinGen Allele Registry
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Canonical Allele Identifier:
CA197961834
Gene: LINC01492
HGNC
NCBI
Linked Data
dbSNP Id:
rs971932644
gnomAD v2:
9-106024317-A-G
gnomAD v3:
9-103262035-A-G
gnomAD v4:
9-103262035-A-G
MyVariant Identifiers:
chr9:g.106024317A>G (hg19)
chr9:g.103262035A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103262035A>G , CM000671.2:g.103262035A>G
GRCh38
NC_000009.11:g.106024317A>G , CM000671.1:g.106024317A>G
GRCh37
NC_000009.10:g.105064138A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2489T>C
Search 100 bp 5'
Search 100 bp 3'