ClinGen Allele Registry
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Canonical Allele Identifier:
CA15792175
Gene: LINC00331
HGNC
NCBI
Linked Data
dbSNP Id:
rs11840225
gnomAD v2:
13-79410633-A-G
gnomAD v3:
13-78836498-A-G
gnomAD v4:
13-78836498-A-G
MyVariant Identifiers:
chr13:g.79410633A>G (hg19)
chr13:g.78836498A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.78836498A>G , CM000675.2:g.78836498A>G
GRCh38
NC_000013.10:g.79410633A>G , CM000675.1:g.79410633A>G
GRCh37
NC_000013.9:g.78308634A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046869.2:n.111+3442T>C
Search 100 bp 5'
Search 100 bp 3'