ClinGen Allele Registry
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Canonical Allele Identifier:
CA1127548521
Gene: LINC01492
HGNC
NCBI
Linked Data
dbSNP Id:
rs1827344026
gnomAD v3:
9-103262097-T-C
gnomAD v4:
9-103262097-T-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103262097T>C , CM000671.2:g.103262097T>C
GRCh38
NC_000009.11:g.106024379T>C , CM000671.1:g.106024379T>C
GRCh37
NC_000009.10:g.105064200T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2427A>G
Search 100 bp 5'
Search 100 bp 3'