ClinGen Allele Registry
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Canonical Allele Identifier:
CA566857042
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs747772433
gnomAD v2:
6-40321822-C-G
gnomAD v3:
6-40354083-C-G
gnomAD v4:
6-40354083-C-G
MyVariant Identifiers:
chr6:g.40321822C>G (hg19)
chr6:g.40354083C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40354083C>G , CM000668.2:g.40354083C>G
GRCh38
NC_000006.11:g.40321822C>G , CM000668.1:g.40321822C>G
GRCh37
NC_000006.10:g.40429800C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.1924G>C
Search 100 bp 5'
Search 100 bp 3'