ClinGen Allele Registry
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Canonical Allele Identifier:
CA253224635
Gene: LINC00331
HGNC
NCBI
Linked Data
dbSNP Id:
rs977291368
gnomAD v3:
13-78836394-A-T
gnomAD v4:
13-78836394-A-T
MyVariant Identifiers:
chr13:g.79410529A>T (hg19)
chr13:g.78836394A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.78836394A>T , CM000675.2:g.78836394A>T
GRCh38
NC_000013.10:g.79410529A>T , CM000675.1:g.79410529A>T
GRCh37
NC_000013.9:g.78308530A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046869.2:n.111+3546T>A
Search 100 bp 5'
Search 100 bp 3'