ClinGen Allele Registry
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Canonical Allele Identifier:
CA16262725
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs2477757
gnomAD v2:
6-40321778-T-C
gnomAD v3:
6-40354039-T-C
gnomAD v4:
6-40354039-T-C
MyVariant Identifiers:
chr6:g.40321778T>C (hg19)
chr6:g.40354039T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40354039T>C , CM000668.2:g.40354039T>C
GRCh38
NC_000006.11:g.40321778T>C , CM000668.1:g.40321778T>C
GRCh37
NC_000006.10:g.40429756T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.1968A>G
Search 100 bp 5'
Search 100 bp 3'