ClinGen Allele Registry
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Canonical Allele Identifier:
CA15419385
Gene: LINC01411
HGNC
NCBI
Linked Data
dbSNP Id:
rs12659144
gnomAD v2:
5-173777520-T-C
gnomAD v3:
5-174350517-T-C
gnomAD v4:
5-174350517-T-C
MyVariant Identifiers:
chr5:g.173777520T>C (hg19)
chr5:g.174350517T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.174350517T>C , CM000667.2:g.174350517T>C
GRCh38
NC_000005.9:g.173777520T>C , CM000667.1:g.173777520T>C
GRCh37
NC_000005.8:g.173710126T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_125806.1:n.223+13941T>C
Search 100 bp 5'
Search 100 bp 3'