ClinGen Allele Registry
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Canonical Allele Identifier:
CA1869205538
Gene: LINC01492
HGNC
NCBI
Linked Data
dbSNP Id:
rs1827344053
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103262098G>A , CM000671.2:g.103262098G>A
GRCh38
NC_000009.11:g.106024380G>A , CM000671.1:g.106024380G>A
GRCh37
NC_000009.10:g.105064201G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2426C>T
Search 100 bp 5'
Search 100 bp 3'