ClinGen Allele Registry
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Canonical Allele Identifier:
CA197961832
Gene: LINC01492
HGNC
NCBI
Linked Data
dbSNP Id:
rs1024485744
MyVariant Identifiers:
chr9:g.106024311C>T (hg19)
chr9:g.103262029C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103262029C>T , CM000671.2:g.103262029C>T
GRCh38
NC_000009.11:g.106024311C>T , CM000671.1:g.106024311C>T
GRCh37
NC_000009.10:g.105064132C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2495G>A
Search 100 bp 5'
Search 100 bp 3'